Methods for diagnosing and monitoring the status of systemic lupus erythematosus

ABSTRACT

The invention presents a method of diagnosing or monitoring the status of systemic lupus erythematosus (SLE) in a subject or patient comprising detecting the expression of all genes of a diagnostic set in the subject or patient wherein the diagnostic set comprises two or more genes having expression correlated with the classification or status of SLE; and diagnosing or monitoring the status of SLE in the subject or patient by applying at least one statistical method to the expression of the genes of the diagnostic set.

PRIORITY

This application claims the benefit of U.S. Prov. App. No. 60/858,147, filed Nov. 9, 2006, which is incorporated by reference herein in its entirety.

TECHNICAL FIELD

The invention provides for the use of gene expression and statistical analysis to diagnose and monitor the status of systemic lupus erythematosus.

BACKGROUND OF THE INVENTION

Systemic lupus erythematosus (SLE) is an autoimmune rheumatic disease characterized by dysregulation of the immune system and differential expression of genes in immunological pathways. In the United States, SLE affects about 2 million patients and 90% of these patients are female. Targeted tissues and organs include the blood, central nervous system (CNS), joints, kidneys, lungs, skin, and vasculature, Symptoms include abnormal blood panels, arthralgias, atherosclerosis, CNS disorders, infections, joint pain, malaise, rashes, ulcers, and the production of autoantibodies. Since disease severity, symptomology, and response to therapy vary widely, SLE is difficult to diagnose, manage and treat.

As described in USSN 20040033498, SLE clearly involves differential gene expression in SLE patients as compared to normal controls. Two laboratories have reported on the role of the interferon (INF)-α inducible genes in SLE and on high levels of anti-RNA binding protein, anti-Ro antibodies, and renal disease (Baechler et al (2003) PNAS100:2610-2615; Kirou et al (2004) Arthritis and Rheumatism 50:3958-3967). However, low positive correlation between disease activity and IFN-inducible genes, the apparent heterogeneity of SLE patients, and lack of longitudinal studies continue to present challenges for clinicians (Kirou et al. (2005) Arthritis and Rheumatism 52:1491-1503).

These challenges point to a need in the art for better diagnosis, characterization, and follow-up of patients with SLE. To this end, longitudinal data from SLE patients was used with methods for detecting and analyzing gene expression to monitor status, quiescence versus flare, and to classify a patient as having type 1 SLE or type 2 SLE.

SUMMARY

The invention presents methods and compositions for diagnosing and monitoring systemic lupus erythematosus (SLE). The methods use gene expression based on nucleic acid or protein technologies, and statistical methods to classify patients as having type 1 SLE or type 2 SLE and to monitor disease activity, predict flare, and assess the efficacy of treatment administered to the patient.

The invention provides a method of diagnosing or monitoring the status of systemic lupus erythematosus (SLE) in a subject or patient includes detecting the expression of all genes of a diagnostic set in the subject or patient wherein the diagnostic set comprises two or more genes having expression correlated with the classification or status of SLE; and diagnosing or monitoring the status of SLE in the subject or patient by applying at least one statistical method to the expression of the genes of the diagnostic set. In one aspect, the statistical method is a prediction algorithm that produces a number or single value indicative of the status of SLE in the subject or patient. In another aspect, the statistical method further comprises classification of the subject or patient into one of at least two classes of SLE, and is optimized to maximize the separation among longitudinally stable classes of SLE. The method also provides a diagnostic set further comprising at least one gene selected from each of at least two gene clusters selected from cluster 1, cluster 2, cluster 3, cluster 4, cluster 5, cluster 6, cluster 7, cluster 8, cluster 9, cluster 10, cluster 11; cluster 12, cluster 13, cluster 14, and cluster 15 of Table 1. The invention further provides classification of the subject or patient into one of at least two classes of SLE further comprising detecting the expression of two or more gene whose expression correlates with the expression of the IFI27 from about 0.5 to about 1.0 and from about −0.5 to about −1.0 calculated using a Pearson correlation; and classifying a subject or patient as having type 1 or type 2 SLE based on the expression of the two or more genes. In one aspect, one of the two or more genes is selected from Table 2 and the classifying step uses a linear algorithm to produce an interferon response (INFr) score wherein a high IFNr score is correlated with type I SLE and a low IFNr score is correlated with type II SLE. The invention additionally provides at least one linear algorithm producing an IFNr score comprising IFI27+IFI144*(1.1296)+OAS3*(1.8136). The invention still further provides a Pearson correlation that is selected from a range of 0.5, 0.4, 0.3, and 0.2 of the expressed genes.

The invention provides a method of diagnosing or monitoring the status of systemic lupus erythematosus (SLE) in a subject or patient comprising detecting the expression of all genes of a diagnostic set in a subject or patient wherein the diagnostic set includes at least one gene from each of at least two gene clusters selected from cluster 1, cluster 2, cluster 3, cluster 4, cluster 5, cluster 6, cluster 7, cluster 8, cluster 9, cluster 10, cluster 11; cluster 12, cluster 13, cluster 14, and cluster 15 of Table 1; and diagnosing or monitoring the status of SLE in the subject or patient based on expression of the genes in the diagnostic set. In one aspect, the expression of all genes in the diagnostic set is detected using a nucleic acid technology further including hybridization in solution or on a substrate or amplification in a quantitative real-time polymerase chain reaction. In another aspect, expression of all genes is proportional to the amount of RNA isolated from a subject or patient sample further including a body fluid selected from whole blood or a blood fraction, ascites, cerebrospinal fluid, lymph, sputum, and urine or a tissue selected from central nervous system, joints, kidneys, liver, lungs, oral cavity, sinuses, skin, and vasculature obtained by any sampling means selected from aspiration of a body fluid, a biopsy of a tissue or an organ, drawing of peripheral blood, endoscopy, and lavage followed by aspiration.

The invention provides for the use of at least one primer or probe set to detect the expression of each of the genes in the diagnostic set. In one aspect, the primers or probe sets are oligonucleotides selected from natural or synthetic cDNA, genomic DNA, locked nucleic acids, peptide nucleic acids, and RNA and can be used in a diagnostic kit. The invention also provides a method of diagnosing a patient as having a longitudinally stable classification of SLE by detecting the expression of two or more genes whose expression correlates with the expression of the IFI27 from about 0.5 to about 1.0 and from about −0.5 to about −1.0 calculated using Pearson correlation; and diagnosing the patient as having type I or type II SLE based on analyzing the expression of the two or more genes using a statistical method.

The invention further provides for assigning a subject or patient to a clinical trial based on their classification as type I SLE or type 2 SLE.

The invention provides for monitoring the status of SLE in a subject or patient by predicting incipient flare or disease activity, and assessing response to a therapeutic agent administered to the patient or to an immunosuppressant administered to a patient. The invention also provides for screening a subject exhibiting symptoms of a rheumatic disease selected from ankylosing spondylitis, dermatomyositis, autoimmune hepatitis, hepatitis-C (hep-C), polymyalgia rheumatica, polymyositis, rheumatoid arthritis (RA), scleroderma, systemic sclerosis, Sjogren's disease, systemic vasculitis, and Whipple's disease.

The invention provides method of producing a probe set for diagnosing or monitoring SLE in a subject or patient by selecting at least one gene from each of at least two of the gene clusters of Table 1 and at least two genes from Table 2; and producing a probe set consisting of at least one oligonucleotide that detects the expression of each of the selected genes. In one aspect, the probe set is used in a diagnostic kit.

The invention provides a method for predicting flare in a patient diagnosed with SLE by analyzing gene expression in a sample from the patient to produce a gene expression profile wherein a first portion of the analysis includes using expression of at least one gene selected from each of at least two of the clusters 1 through 15 of Table 1 and at least one statistical method to produce a patient expression profile, and a second portion of the analysis includes using expression of at least two genes selected from Table 2 and a linear algorithm to classify the patient as having type 1 SLE or type 2 SLE; and predicting flare by comparing the patient gene expression profile at least one reference profile. In one aspect, the reference profile is selected from at least one normal subject, at least one patient classified as having type 1 SLE with quiescent status, at least one patient classified as having type 1 SLE in flare, at least one patient classified as having type 2 SLE with quiescent status, at least one patient classified as having type 2 SLE in flare.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 shows the Log₁₀ expression ration for Interferon Responsive Gene IFI27 in QF and F paired samples.

FIG. 2 shows the Interferon Response (INFr) score for normal controls and SLE patient.

FIG. 3 shows the bimodal distribution for IFI27, IFI44, and OAS3 of SLE patients.

DESCRIPTION OF THE TABLES

Table 1 shows 15 clusters of correlated genes that are differentially expressed as SLE patients change status from quiescence to flare and can be used with at least one statistical method to predict flare. Cell types corresponding to each cluster are indicated as well as Array ID, Genbank ID, Gene ID, and the source of each gene. 60-mer sequences, which are unique identifiers for the genes, are also displayed in Table 1. The Sequence Listing provides the 60-mer sequences listed in Table 1.

Table 2 lists INFr genes with expression that positively correlates with IFI27 expression and can be used with at least one statistical method to classify a patient as having either type 1 SLE or type 2 SLE. 60-mer sequences, which are unique identifiers for the genes, are also displayed in Table 2.

Table 3 presents longitudinal data for SLE patients showing stability in an individual's INFr score and its lack of correlation with SLEDAI.

DETAILED DESCRIPTION OF THE INVENTION

Definitions

Unless defined otherwise, all scientific and technical terms are understood to have the same meaning as commonly used in the art to which they pertain. In this application, the singular form—“a”, “an”, and “the”—includes plural references unless the context clearly dictates otherwise. For example, the term “an agent” includes a plurality of agents and mixtures thereof. For the purpose of this invention, the following terms are defined below.

“Amplification” refers to any device, method or technique that can make copies of a nucleic acid. It can be achieved using polymerase chain reaction (PCR) techniques such as linear amplification (cf. U.S. Pat. No. 6,132,997), rolling circle amplification, and the like. Further, amplification and detection can be combined as in TAQMAN Real-Time PCR(RT-PCR) using the TAQMAN protocols and the Prism 7900HT Sequence detection system and software (Applied Biosystems (ABI), Foster City Calif.).

“Array” refers to an ordered arrangement of at least two reagents—antibodies, nucleic acids or proteins—in solution or on a substrate where at least one of the reagents represents a normal control and the other, a sample of diagnostic or prognostic interest. The ordered arrangement insures that the size and signal intensity of each labeled complex, formed between at least one reagent and at least one nucleic acid or protein to which the reagent specifically binds, is individually distinguishable.

The term “diagnostic set” generally refers to a set of two or more genes that, when evaluated for differential expression of their products, collectively yields predictive data. Such predictive data typically relates to diagnosis, prognosis, monitoring of therapeutic outcomes, and the like. In general, the components of a diagnostic set are distinguished from nucleotide sequences that are evaluated by analysis of the DNA to directly determine the genotype of an individual as it correlates with a specified trait or phenotype, such as a disease, in that it is the pattern of expression of the components of the diagnostic set, rather than mutation or polymorphism of the DNA sequence that provides predictive value. It will be understood that a particular component (or member) of a diagnostic set can, in some cases, also present one or more mutations, or polymorphisms that are amenable to direct genotyping by any of a variety of well known analysis methods, e.g., Southern blotting, RFLP, AFLP, SSCP, SNP, and the like.

“cDNA” refers to an isolated polynucleotide, nucleic acid molecule, or any fragment or complement thereof that originated recombinantly or synthetically, is double- or single-stranded, represents coding and noncoding 3′ or 5′ sequence, and generally lacks introns.

“Classification” refers to the categorization of a subject or patient based on gene expression as having type 1 SLE or type 2 SLE. SLE is considered to be type 1 if it primarily involves Type 1 T helper cells and type 1-linked cytokines, such as interferon-gamma. SLE is considered to be type 2 if there is more involvement of Type 2 helper cells which activate an antibody-driven immune response.

“Expression” refers differential gene expression—an increased (i.e., upregulated) or a decreased (i.e., downregulated) expression as detected by absence, presence, or change in the amount of messenger RNA or protein for a gene in a sample.

“Flare” refers to onset of disease activity in a patient diagnosed with an immune disorder; in SLE, mild flare has been defined by an increase in systemic lupus erythematosus disease activity index (SLEDAI) by ≧four units over a previous score for that patient and severe flare, as an increase in SLEDAI by ≧12 units. SLEDAI represents a composite assessment of disease activity based on 16 clinical manifestations and eight laboratory measures including two immunological tests with a possible range of overall score from 0 to 105.

A “gene expression profile” refers to the identification, characterization, quantification, and representation of a plurality of genes expressed in a sample as measured using nucleic acid or protein technologies. A nucleic acid expression profile is produced using mature mRNA transcript and/or regulatory sequences such as promoters, enhancers, introns, mRNA-processing intermediates, and 3′ untranslated regions in nucleic acid technologies. A protein expression profile, although time delayed, mirrors the nucleic acid expression profile and is produced using protein technologies and proteins and/or antibodies to detect protein expression in a sample. Results from subject or patient samples are compared with reference profiles based on normal, diseased, or treated samples.

“Immunosuppressant” refers to any therapeutic agent that suppresses immune response in a patient such as anticoagulents, antimalarials, heart drugs, non-steroidal anti-inflammatory drugs (NSAIDs), and steroids including but not limited to aspirin, azathioprine, chloroquine, corticosteroids, cyclophosphamide, cyclosporin A, dehydroepiandrosterone, deoxyspergualin, dexarnethasone, everolimus, fenoprofen, hydralazine, hydroxychloroquine, immunoglobulin, ibuprofen, indomethacin, leflunomide, ketoprofen, meclophenamate, mepacrine, 6-mercaptopurine, methotrexate, mizoribine, mycophenolate mofetil, naproxen, prednisone, methyprenisone, rapamycin (sirolimus), solumedrol, tacrolimus (FK506), thymoglobulin, tolmetin, tresperimus, triamcinoline, and the like.

“Longitudinally stable” refers to the behavior of one or more interferon response (INFr) genes expressed in samples collected at different time points from an individual or data derived from those samples.

“Diagnosis or monitoring” refers to the detection of gene expression at the nucleic acid or protein level to provide useful information about an individual's medical status, Monitoring status can include determination of prognosis or complication, following progression of a disease, prediction of disease activity or flare, providing information relating to a patient's health over a period of time, selection of a therapeutic agent and/or determining response or resistance to that agent, selecting an individual patient or small subsets of patients most likely to benefit from an experimental therapy or clinical trial, and determining classification of a patient as having a particular disease status.

“Normal” refers to the medical status of an individual, or a sample from an individual, who does not have SLE or any diagnosis or manifestation of an infection or immune disorder and can be used as a negative control.

“Nucleic acid technology” refers to any device, means or system used to detect gene expression or produce a gene expression profile and includes but is not limited to methods using arrays for amplification in PCR, TAQMAN RT-PCR, quantitative RT-PCR, and the like, or hybridization in solution or on a substrate containing cDNAs, genomic DNAs, locked nucleic acids, oligonucleotide primers or probes, peptide nucleic acids, polynucleotides, and RNAs of any length either natural or synthetic, and the like.

“Patient” refers to a human subject who is genetically predisposed to a rheumatic disease or has been diagnosed with a SLE.

“Prediction” refers to the use of gene expression assessed using nucleic acid or protein technologies, algorithms and statistical analyses to provide information about an individual's status; for example, being predisposed to, diagnosed with, or effectively treated for disease activity or flare.

“Protein technology” includes but is not limited to activity assays, affinity antibody or protein arrays, chromatographic separation, calorimetric assays, two-dimensional gel electrophoresis, enzyme-linked immunosorbent assays (ELISA), fluorescent-activated cell sorting (FACS), mass spectrophotometric detection, western analysis, and the like.

A “reference profile” refers to gene expression or gene expression profiles from well-characterized normal, diseased or treated samples taken from at least one subject and giving repeatable results whenever used in or with a particular nucleic acid or protein technology.

A “rheumatic disease” is a condition or disorder selected from ankylosing spondylitis, dermatomyositis, autoimmune hepatitis, hepatitis-C (hep-C), polymyalgia rheumatica, polymyositis, rheumatoid arthritis (RA), scleroderma, systemic sclerosis, Sjogren's disease, systemic vasculitis, Whipple's disease and the like.

“Sample” is used in its broadest sense and refers to any biological material used to obtain histological information or to measure gene expression obtained by any means from a subject. A sample can be a body fluid such as ascites, bile, blood, cerebrospinal fluid, synovial fluid, lymph, pus, semen, sputum, urine; the soluble fraction of a cell preparation, an aliquot of media in which cells were grown; a chromosome, an organelle, or membrane isolated or extracted from a cell; cDNA, genomic DNA, or RNA in solution or bound to a substrate; a cell; a tissue biopsy, and the like, Preferred samples for diagnosis, prognosis, or monitoring of SLE patients are leukocytes or serum derived from whole blood, biopsies of the central nervous system (CNS), joints, kidneys, liver, lungs, oral cavity, sinuses, skin, vasculature, and any other tissues or organs affected by SLE.

“Sampling means” refers to aspiration, biopsy, endoscopy, lavage, needle aspiration or biopsy, puncturing with a lancet; bleeding, ejaculating, expectorating, seeping, or urinating into or onto a collection device, container, substrate, and the like.

“Status” refers to the deterioration, improvement, progression, remission, or stability of a patient with SLE, as determined from analyzing one or more samples from that patient. Status, or a change therein, can be used to evaluate the need for administration of a therapeutic agent, to adjust dosage of such an agent, to change or use another agent or treatment regime, and the like.

“Statistical methods” include but are not limited to analysis of variance, classification algorithms, classification and regression trees, Fisher's Exact Test, linear algorithm, linear discriminatory analysis, linear regression, logistic algorithm, multiple regression, nearest shrunken centroids classifier, Pearson correlation, prediction algorithm, significance analysis of microarrays, one-tailed T-tests, two-tailed T-tests, voting algorithm, Wilcoxon's signed ranks test, and the like.

“Substrate” refers to any rigid or semi-rigid support to which antibodies, nucleic acids or proteins are bound and includes magnetic or nonmagnetic beads, capillaries or other tubing, chips, fibers, filters, gels, membranes, microparticles, plates, polymers, slides, and wafers with a variety of surface forms including channels, columns, pins, pores, trenches, wells and the like.

“Therapeutic agent” refers to any pharmaceutical molecule or compound that will bind specifically to a polynucleotide or to an epitope of a protein and stabilize or modulate the activity of the polynucleotide or protein. It can be composed of inorganic and/or organic substances including minerals, cofactors, nucleic acids, proteins, carbohydrates, fats, and lipids and includes but is not limited to Ace inhibitors, aspirin, azathioprine, B7RP-1-fc, β-blockers, brequinar sodium, campath-1H, celecoxib, chloroquine, corticosteroids, coumadin, cyclophosphamide, cyclosporin A, dehydroepiandrosterone, deoxyspergualin, dexamethasone, diclofenac, dolobid, etodolac, everolimus, FK778, feldene, fenoprofen, flurbiprofen, heparin, hydralazine, hydroxychloroquine, CTLA-4 or LFA3 immunoglobulin, ibuprofen, indomethacin, ISAtx-247, ketoprofen, ketorolac, leflunomide, meclophenamate, mefenamic acid, mepacrine, 6-mercaptopurine, meloxicam, methotrexate, mizoribine, mycophenolate mofetil, naproxen, oxaprozin, Plaquenil, NOX-100, prednisone, methyprenisone, rapamycin (sirolimus), sulindac, tacrolimus (FK506), thymoglobulin, tolmetin, tresperimus, U0126, and antibodies including but not limited to alpha lymphocyte antibodies, adalimumab, anti-CD3, anti-CD25, anti-CD52 anti-IL2R, and anti-TAC antibodies, basiliximab, daclizumab, etanercept, hu5C8, infliximab, OKT4, natalizumab and the like.

DETAILED DESCRIPTION OF THE INVENTION

Description

Microarray experiments have been used to find genes that are differentially expressed in patients diagnosed with systemic lupus erythrematosus (SLE). These genes were described in U.S. Pat. No. 6,905,827 and U.S. Ser. No. 10/990,298, each incorporated by reference herein in its entirety.

The invention provides methods of diagnosing or monitoring the status of SLE in a subject or patient by detecting the expression of all genes of a diagnostic set in the subject or patient wherein the diagnostic set has two or more genes having expression correlated with the classification or status of SLE; and diagnosing or monitoring the status of SLE in the subject or patient by applying at least one statistical method to the expression of the genes of the diagnostic set.

The methods of the invention also include classifying the subject or patient as having type 1 SLE or type 2 SLE, predicting flare, and monitoring disease activity and treatment efficacy.

Diagnostic Genes of the Invention

The invention provides diagnostic sets containing genes that can be used to diagnosis and monitor SLE disease status. The diagnostic sets can also be used to predict occurrence and future complication of the disease.

Diagnostic genes were identified and validated for use in diagnosing and monitoring of SLE status by identifying genes for which a correlation exists between the SLE status of an individual as determined based on various disease criteria and the individual's expression of RNA or protein products corresponding to the gene. Disease criteria may include clinical data such as symptom rash, joint pain, malaise, rashes, blood counts (white and red), tests of renal function (e.g. creatinine, blood urea nitrogen, creative clearance), data obtained from laboratory tests, including complete blood counts with differentials, CRP, ESR, ANA, Serum IL6, Soluble CD40 ligand, LDL, HDL, Anti-DNA antibodies, rheumatoid factor, C3, C4, serum creatinine and any medication levels, the need for pain medications, cumulative doses or immunosuppressive therapy, symptoms or any manifestation of carotid atherosclerosis (e.g. ultrasound diagnosis or any other manifestations of the disease), data from surgical procedures such as gross operative findings and pathological evaluation of resected tissues and biopsies (e.g., renal, CNS), information on pharmacological therapy and treatment changes, clinical diagnoses of disease “flare”, hospitalizations, death, response to medications, quantitative joint exams, results from health assessment questionnaires (HAQs), and other clinical measures of patient symptoms and disability. Disease criteria also include the clinical score known as SLEDAI (Bombadier C, Gladman D D, Urowitz M B, Caron D, Chang C H and the Committee on Prognosis Studies in SLE: Derivation of the SLEDAI for Lupus Patients. Arthritis Rheum 35:630-640, 1992.).

The diagnostic genes of this invention include sequences corresponding those provided by the accession numbers and Unigene numbers provided in Table 1 and 2. The 60-mer sequences provided in the Tables are unique identifiers for the diagnostic genes of this invention. Therefore, the diagnostic genes of this invention also include sequences containing the 60-mer sequence provided in the Tables. In other words, the diagnostic genes may be partially or totally contained in (or derived from) the full-length gene sequences referenced in Tables 1 and 2.

In certain embodiments, the diagnostic genes of this invention include any sequences whose expression correlates with the expression of all genes which correlate with IFI27, such as the sequences provided by the accession numbers and Unigene numbers provided in Table 2.

Homologs and variants of the nucleic acid molecules in Table 1 and Table 2 may also be part of the diagnostic gene set. Homologs and variants of these nucleic acid molecules will possess a relatively high degree of sequence identity when aligned using standard methods. The sequences encompassed by the invention have at least 40-50, 50-60, 70-80, 80-85, 85-90, 90-95, or 95-100% sequence identity to the sequences disclosed herein.

The diagnostic gene set may also include other genes that are coexpressed with the correlated sequence or full-length gene. Genes may share expression patterns because they are regulated in the same molecular pathway or in the same cell type. Because of the similarity of expression behavior, these genes are identified as surrogates in that they can substitute for a diagnostic gene in a diagnostic gene set.

In some embodiments, diagnostic genes of the invention are used as a diagnostic gene set in combination with genes that are known to be associated with a disease state (“known markers”). The use of the diagnostic genes in combination with the known markers can provide information that is not obtainable through the known markers alone.

Gene Clusters

In some embodiments, the diagnostic genes of this invention are segregrated into “clusters”. In preferred embodiments the diagnostic genes of this invention are sorted into clusters as indicated in Table 1 and diagnostic gene sets of this invention include at least one gene from each of at least two of gene clusters 1 through 15.

As used herein the term “gene cluster” or “cluster” refers to a group of genes related by expression pattern. In other words, a cluster of genes is a group of genes with similar regulation across different conditions, such as a patient having SLE or a patient without SLE. The expression profile for each gene in a cluster should be correlated with the expression profile of at least one other gene in that cluster. Correlation may be evaluated using a variety of statistical methods.

As used herein the term “surrogate” refers to a gene with an expression profile such that is so highly correlated with gene expression of another gene that it can substitute for a diagnostic gene in a diagnostic assay. Such genes are typically members of the same gene cluster as the diagnostic gene. For each member of a diagnostic gene set, a set of potential surrogates can be identified through identification of genes with similar expression patterns as described below.

Many statistical analyses produce a correlation coefficient to describe the relatedness between two gene expression patterns. Patterns may be considered correlated if the correlation coefficient is greater than or equal to 0.8. In preferred embodiments, the correlation coefficient should be greater than 0.85, 0.9 or 0.95. Other statistical methods produce a measure of mutual information to describe the relatedness between two gene expression patterns. Patterns may be considered correlated if the normalized mutual information value is greater than or equal to 0.7. In preferred embodiments, the normalized mutual information value should be greater than 0.8, 0.9 or 0.95. Patterns may also be considered similar if they cluster closely upon hierarchical clustering of gene expression data (Eisen et al. 1998). Similar patterns may be those genes that are among the 1, 2, 5, 10, 20, 50 or 100 nearest neighbors in a hierarchical clustering or have a similarity score (Eisen et al. 1998) of >0.5, 0.7, 0.8, 0.9, 0.95 or 0.99. Similar patterns may also be identified as those genes found to be surrogates in a classification tree by CART (Breiman et al. 1994).

Often, but not always, members of a gene cluster have similar biological functions in addition to similar gene expression patterns. For example, all genes in a particular cluster may be associated with a particular biological pathway or cell type. Representative cell types associated with diagnostic genes of this invention include granulocytes, NK cells, red blood cells, and platelets. Is is expected that the expression pattern of other genes in the same pathway or cell type will also be part of the same cluster and may be useful as surrogates.

Correlated genes, clusters and surrogates are all useful as diagnostic genes of the invention. These surrogates may be used as diagnostic genes in an assay instead of, or in addition to, the diagnostic genes for which they are surrogates.

Clusters also provide a means to ensure that the diagnostic gene sets do not contain redundant information. Diagnostic gene sets of the invention therefore preferably include genes from different clusters. For example, diagnostic gene sets of the invention preferably include at least one gene from at least two gene clusters.

Primer and Probe Sets

The invention further provides methods for producing diagnostic primer sets or probe sets. It is understood that a probe includes any reagent capable of specifically identifying genes in diagnostic setss, and include but are not limited to DNA, RNA, cDNA, splice variants, primers, probe sets, peptide nucleic acids, locked nucleic acids, amplicons, synthetic oligonucleotide, and partial or full-length nucleic acid sequences. In addition, the probe may identify the protein product of a diagnostic gene, and include, for example, antibodies and other affinity reagents. In some applications, a probe set may include one or more oligonucleotide that detects the expression of one or more of the selected genes for the diagnostic set.

It is also understood that each probe can correspond to one gene, or multiple probes can correspond to one gene, or both, or one probe can correspond to more than one gene.

In some embodiments, a diagnostic probe set is immobilized on an array. The array may be a chip array, a plate array, a bead array, a pin array, a membrane array, a solid surface array, a liquid array, an oligonucleotide array, a polynucleotide array or a cDNA array, a microtiter plate, a pin array, a bead array, a membrane or a chip.

Obtaining DNA, RNA and Protein Samples for Detection of Expression

Gene expression can be evaluated at the level of DNA, or RNA or protein products. A variety of techniques are available for the isolation of DNA, RNA and protein from bodily fluids.

A variety of techniques are available for the isolation of RNA from samples. Any technique that allows isolation of mRNA from cells (in the presence or absence of rRNA and tRNA) can be utilized. For example, by means of aspiration of body fluid, biopsy of a tissue or organ, drawing of peripheral blood, endoscopy, and lavage followed by aspiration, RNA can be isolated from ascites, bile, blood, cerebronspinal fluid, lymph, sputum, and/or urine. By the same methods, RNA can also be isolated from the central nervous system, joints, kidneys, liver, lungs, oral cavity, sinuses, skin, and vasculature.

Methods for Obtaining Expression Data

Numerous methods for obtaining expression data are known, and any one or more of these techniques, singly or in combination, are suitable for detecting expression in the context of the present invention.

For example, expression patterns can be evaluated by northern analysis, PCR, RT-PCR, Taq Man analysis, FRET detection, monitoring one or more molecular beacons, hybridization to an oligonucleotide array, hybridization to a cDNA array, hybridization to a polynucleotide array, hybridization to a liquid microarray, hybridization to a microelectric array, cDNA sequencing, clone hybridization, cDNA fragment fingerprinting, serial analysis of gene expression (SAGE), subtractive hybridization, differential display and/or differential screening (see, e.g., Lockhart and Winzeler (2000) Nature 405:827-836, and references cited therein). Oligonucleotide hybridization may occur in solution or on substrates including, but not limited to magnetic or nonmagnetic beads, chips, fibers, filters, gels, membranes, microparticles, plates, polymers, slides, capillary tubing, and wafers with surface features selected from channels, columns, pins, pores, trenches, and wells.

It is understood that for detection of gene expression, variations in the disclosed sequences will still permit detection of gene expression. The degree of sequence identity required to detect gene expression varies depending on the length of the oligomer. For a 60 mer, 6-8 random mutations or 6-8 random deletions in a 60 mer do not affect gene expression detection. Hughes, T R, et al. “Expression profiling using microarrays fabricated by an ink-jet oligonucleotide synthesizer. Nature Biotechnology, 19:343-347 (2001). As the length of the DNA sequence is increased, the number of mutations or deletions permitted while still allowing the detection of gene expression is increased.

Alternatively, expression at the level of protein products of gene expression can be performed. For example, protein expression in a disease patient can be evaluated by one or more methods including, but not limited to Western analysis, two-dimensional gel analysis, chromatographic separation, mass spectrometric detection, protein-fusion reporter constructs, calorimetric assays, binding to a protein array and characterization of polysomal mRNA. One particularly favored approach involves binding of labeled protein expression products to an array of antibodies specific for members of the candidate library. Methods for producing and evaluating antibodies are widespread in the art, see, e.g., Coligan, supra; and Harlow and Lane (1989) Antibodies: A Laboratory Manual, Cold Spring Harbor Press, NY (“Harlow and Lane”). Additional details regarding a variety of immunological and immunoassay procedures adaptable to the present invention by selection of antibody reagents specific for the products of candidate nucleotide sequences can be found in, e.g., Stites and Terr (eds.)(1991) Basic and Clinical Immunology, 7.sup.th ed., and Paul, supra. Another approach uses systems for performing desorption spectrometry. Commercially available systems, e.g., from Ciphergen Biosystems, Inc. (Fremont, Calif.) are particularly well suited to quantitative analysis of protein expression. Indeed, Protein Chip® arrays (see, e.g., the website, ciphergen.com) used in desorption spectrometry approaches provide arrays for detection of protein expression. Alternatively, affinity reagents (e.g., antibodies, small molecules, etc.) are developed that recognize epitopes of the protein product. Affinity assays are used in protein array assays, e.g. to detect the presence or absence of particular proteins. Alternatively, affinity reagents are used to detect expression using the methods described above. In the case of a protein that is expressed on the cell surface of leukocytes, labeled affinity reagents are bound to populations of leukocytes, and leukocytes expressing the protein are identified and counted using fluorescent activated cell sorting (FACS).

Expression Profiles

Expression patterns, or profiles, of a plurality of genes corresponding to members of the diagnostic set are evaluated in one or more SLE patients. These expression patterns constitute a set of relative or absolute expression values for some number of RNA or protein products corresponding to the plurality of genes evaluated, which is referred to herein as the subject's “expression profile” for those genes. While expression patterns for as few as one independent member of the diagnostic set can be obtained, it is generally preferable to obtain expression patterns corresponding to a larger number of genes, e.g., about 2, about 5, about 10, about 20, about 50, about 100, about 200, about 500, or about 1000, or more. The expression pattern for each differentially expressed component member of the set provides a finite specificity and sensitivity with respect to predictive value, e.g., for diagnosis, prognosis, monitoring, and the like.

Evaluation of Expression Data and Profiles

Expression profiles can be evaluated by qualitative and/or quantitative measures. Certain techniques for evaluating gene expression (as RNA or protein products) yield data that are predominantly qualitative in nature. That is, the methods detect differences in expression that classify expression into distinct modes without providing significant information regarding quantitative aspects of expression. For example, a technique can be described as a qualitative technique if it detects the presence or absence of expression of a diagnostic nucleotide sequence, i.e., an on/off pattern of expression. Alternatively, a qualitative technique measures the presence (and/or absence) of different alleles, or variants, of a gene product.

In contrast, some methods provide data that characterizes expression in a quantitative manner. That is, the methods relate expression on a numerical scale. It will be understood that the numerical, and symbolic examples provided are arbitrary, and that any graduated scale (or any symbolic representation of a graduated scale) can be employed in the context of the present invention to describe quantitative differences in nucleotide sequence expression. Typically, such methods yield information corresponding to a relative increase or decrease in expression.

Any method that yields either quantitative or qualitative expression data is suitable for evaluating expression of diagnostic nucleotide sequence in a SLE subject or patient. In some cases, e.g., when multiple methods are employed to determine expression patterns for a plurality of diagnostic nucleotide sequences, the recovered data, e.g., the expression profile for the nucleotide sequences is a combination of quantitative and qualitative data.

In some applications, expression of the plurality of diagnostic nucleotide sequences is evaluated sequentially. This is typically the case for methods that can be characterized as low- to moderate-throughput. In contrast, as the throughput of the elected assay increases, expression for the plurality of diagnostic nucleotide sequences in a sample or multiple samples of SLE subjects or patients is assayed simultaneously. Again, the methods (and throughput) are largely determined by the individual practitioner, although, typically, it is preferable to employ methods that permit rapid, e.g. automated or partially automated, preparation and detection, on a scale that is time-efficient and cost-effective.

In one some embodiments, once expression levels for a diagnostic set of genes are determined, a diagnostic classifier (a mathematical function that assigns samples to diagnostic categories based on expression data) is applied to unknown sample expression levels in order to diagnose or monitor the status of the SLE in a subject or patient.

The diagnostic classifier is typically derived from a prediction algorithm derived from statistical methods including, but not limited to, analysis of variance, classification algorithms, classification and regression trees, Fisher's Exact Test, linear algorithm. linear discriminatory analysis, linear regression, logistic algorithm, multiple regression, nearest shrunken centroids classifier, Pearson correlation, prediction algorithm, significance analysis of microarrays, one-tailed T-test, two tailed T-tests, voting algorithm, Wilcoxon's signed ranks test and the like.

Expression Reference Standards

In other embodiments, comparison of patient gene expression with reference profiles is used to evaluate expression data and to monitor the status of SLE, to predict flare, and to assess treatment efficacy.

For example, expression profiles derived from a patient (i.e., subjects diagnosed with, or exhibiting symptoms of, or exhibiting a disease criterion, or under a doctor's care for a disease) sample are compared to a control or standard expression RNA to facilitate comparison of expression profiles (e.g. of a set of candidate nucleotide sequences) from a group of patients relative to each other (i.e., from one patient in the group to other patients in the group, or to patients in another group).

The reference RNA used should have desirable features of low cost and simplicity of production on a large scale. Additionally, the reference RNA should contain measurable amounts of as many of the genes of the candidate library as possible.

For example, in one approach to identifying diagnostic gene sets and evaluating expression data, expression profiles derived from patient samples are compared to an expression reference “standard.” Standard expression reference can be derived from samples from at least one normal subject and from at least one patient diagnosed with SLE and include but are not limited to a gene expression from one or more patients with quiescent type 1 SLE, from one or more patients with quiescent type 2 SLE, from one or more patients with type 1 SLE showing increased disease activity or flare, from one or more patients with type 2 SLE showing increased disease activity or flare, from one or more patients with type 1 SLE that had been treated with an immunosuppressant, from one or more patients with type 2 SLE that had been treated with an immunosuppressant, from one or more patients with type 1 SLE that had been treated with a therapeutic agent, and from one or more patients with type 2 SLE that had been treated with a therapeutic agent.

Use of an expression reference standard is particularly useful when the expression of large numbers of nucleotide sequences is assayed, e.g. in an array, and in certain other applications, e.g. qualitative PCR, RT-PCR, etc., where it is desirable to compare a sample profile to a standard profile, and/or when large numbers of expression profiles, e.g. a patient population, are to be compared. Generally, an expression reference standard should be available in large quantities, should be a good substrate for amplification and labeling reactions, and should be capable of detecting a large percentage of candidate nucleic acids using suitable expression profiling technology.

Alternatively, the expression reference standard can be derived from any subject or class of subjects including healthy subjects or subjects diagnosed with the same or a different disease or disease criterion. Expression profiles from subjects in two distinct classes are compared to determine which subset of genes in the diagnostic set best distinguish between the two subject classes. It will be appreciated that in the present context, the term “distinct classes” is relevant to at least one distinguishable criterion relevant to a disease of interest, a “disease criterion.” The classes can, of course, demonstrate significant overlap (or identity) with respect to other disease criteria, or with respect to disease diagnoses, prognoses, or the like. The mode of discovery involves, e.g., comparing the molecular signature of different subject classes to each other (such as patient to control, patients with a first diagnosis to patients with a second diagnosis, etc.) or by comparing the molecular signatures of a single individual taken at different time points. The invention can be applied to a broad range of diseases, disease criteria, conditions and other clinical and/or epidemiological questions, as further discussed above/below.

In some applications, when a single patient sample is obtained, it may still be desirable to compare the expression profile of that sample to some reference expression profile. In this case, one can determine the change of expression between the patient's sample and a reference expression profile that is appropriate for that patient and the medical condition in question. For example, a reference expression profile can be determined for all patients without the disease criterion in question who have similar characteristics, such as age, sex, race, diagnoses, etc.

Classification of SLE Patients into Longitudinally Stable Classes of SLE

In some embodiments, the invention provides methods for diagnosis of a patient as having a longitudinally stable classification of SLE by detecting the expression of genes whose expression correlates with the expression of IFI27. In some embodiments, the method is practiced as part of a method to diagnose or monitor the status of SLE in a patient.

In preferred embodiments, a subject is classified into one of at least two classes of SLE by detecting the expression of at least two genes whose expression corrrelates with the expression of IFI27 from about 0.5 to about 1.0 and from about −0.5 to about −1.0 calculated using Pearson correlation and classifying the subject as having type I or type II SLE based on the expression of these two genes. In preferred embodiments, the genes are provided in Table 2.

Pharmacogenomics

Pharmocogenomics is the study of the individual propensity to respond to a particular drug therapy (combination of therapies). In this context, response can mean whether a particular drug will work on a particular patient, e.g. some patients respond to one drug but not to another drug. Response can also refer to the likelihood of successful treatment or the assessment of progress in treatment. Titration of drug therapy to a particular patient is also included in this description, e.g. different patients can respond to different doses of a given medication. This aspect may be important when drugs with side-effects or interactions with other drug therapies are contemplated.

Diagnostic gene sets are developed and validated for use in assessing whether a patient will respond to a particular therapy and/or monitoring response of a patient to drug therapy (therapies). Disease criteria correspond to presence or absence of clinical symptoms or clinical endpoints, presence of side-effects or interaction with other drug(s). The diagnostic nucleotide set may further include nucleotide sequences that are targets of drug treatment or markers of active disease.

Example 1 describes the SLE patients, criteria for their diagnosis, and collection and characterization of blood and tissue samples from normal subjects and patients in periods of quiescence and flare. Although analyses determined that expression profiles contained a subset of genes, designated interferon response genes (INFr), whose expression generally correlated with disease severity, but not with change in patient status from quiescence to flare. Based on this fact, subject and patient samples can be queried for expression of the subset of INFr genes.

Example 2 describes the analysis of gene expression in samples from SLE patients. Pearson correlation was used to identify 15 different, pathway or cell-type specific, gene clusters that were differentially expressed in patient samples during periods of disease quiescence versus periods when that patient was converting from quiescence to flare. These clusters are also shown and described in Table 1. Column 1 shows the number of the cluster; column 2, the array ID; column 3, the GenBank ID; column 4, the gene ID; and column 5, a short description of the gene.

To diagnose and monitor the status of a subject or patient, a sample from the subject or patient is analyzed for differential expression of at least one gene selected from each of at least two different gene clusters shown in Table 1. Comparison of patient gene expression with reference profiles can also serve to monitor the status of SLE, to predict flare, and to assess treatment efficacy.

Prediction algorithms were developed using gene expression representing quiescent (QQ) versus flare (QF) samples. Multiple regression analysis was used to associate gene expression with flare, and linear regression was used to examine individual genes. In general, prediction algorithms were trained using 90% of the samples; and cross-validated, using 10% of samples in 100 iterations as explained in Example 3. Prediction algorithms can be also used to assess patient prognosis—presence or likelihood of developing premature carotid atherosclerosis or progressing to end-stage organ damage—and to monitor treatment of SLE patients. Of particular interest are samples and expression profiles from patients who responded to a given steroid or immunosuppressant treatment regime versus samples or profiles from those same patients where the medication stopped working or from different patients who did not respond or were resistant to a specific medication or treatment regime.

Gene expression was analyzed using at least one statistical method selected from analysis of variance, classification algorithms, classification and regression trees, Fisher's Exact Test, linear algorithm, linear discriminatory analysis, linear regression, logistic algorithm, multiple regression, nearest shrunken centroids classifier, Pearson correlation, prediction algorithm, significance analysis of microarrays, one-tailed T-tests, two-tailed T-tests, voting algorithm, Wilcoxon's signed ranks test and the like. One or more of these methods were used to process and evaluate the normal and patient samples and to choose those samples used as reference profiles.

Example 4 describes the classification of SLE patients into type 1 SLE and type 2 SLE is based on IFNr score. A linear algorithm was used in the analysis of the expression of at least two INFr genes selected from Table 2. Expression of IFI27 was chosen as the basis to which all of other genes expressed in SLE were compared, and Table 2 shows the 190 features (probes on a microarray) that represent those INFr genes positively correlated with IFI27 (cutoff of ≧0.5 or <−0.5 using Pearson correlation). Column 1 of Table 2 shows the feature ID on the Human Genome CGH 44A microarrays (Agilent Technologies, Palo Alto Calif.) array; column 2, the name of probe; column 3, symbol or identifier for the gene; column 5, description of the gene; and column 6, correlation with IFI27. For purposes of demonstration, IFI27 and the two other INFr genes highlighted in Table 2 were used to develop an exemplary algorithm, IFI27+IFI144*(1.1296)+OAS3*(1.8136), that can be used to produce an INFr score.

The analysis and validation of data from paired, longitudinal samples as described in Example 4 are summarized in Table 3. Exemplary data is shown for the first 25 of 81 patients. The data shows lack of correlation with SLEDAI and the stability of IFNr score in individual patients during periods of quiescence and flare. Regardless of disease activity or flare, a high INFr score classified a patient as having type 1 SLE, a condition characterized by more severe SLE symptoms such as increased organ involvement and dysfunction, low complement levels, and high titer of anti-double-stranded DNA (dsDNA) antibodies; and a low INFr score classified a patient as having type 2 SLE which is generally characterized by less severe symptoms. It is contemplated that many combinations of at least two INFr genes and algorithms developed using them can be used to classify SLE patients.

Examples 5-8 describe how normal and patient samples were purified and handled. Examples 9-11 describe the nucleic acid technologies (microarray and polymerase chain reaction) used to detect gene expression and produce gene expression patient and reference profiles.

Methods are presented for screening subjects for SLE, for classifying a patient already diagnosed with SLE as having type 1 SLE or type 2 SLE, for predicting disease activity or flare, for selecting an effective immunosuppressant and/or therapeutic agent for treatment of SLE, and for identifying subjects with SLE from subjects with other rheumatic diseases.

Useful reference profiles were derived from samples from at least one normal subject and from at least one patient diagnosed with SLE and include but are not limited to a gene expression from one or more patients with quiescent type 1 SLE, from one or more patients with quiescent type 2 SLE, from one or more patients with type I SLE showing increased disease activity or flare, from one or more patients with type 2 SLE showing increased disease activity or flare, from one or more patients with type I SLE that had been treated with an immunosuppressant, from one or more patients with type 2 SLE that had been treated with an immunosuppressant, from one or more patients with type 1 SLE that had been treated with a therapeutic agent, and from one or more patients with type 2 SLE that had been treated with a therapeutic agent.

Reagents used to establish a gene expression profile include but are not limited to:

1) genes and their splice variants, primers, probe sets, peptide nucleic acids, locked nucleic acids and amplicons that can be used in nucleic acid technologies including but not limited to hybridization on arrays and amplification using quantitative RT-PCR; and 2) proteins and their fragments, antibodies, and affinity reagents that can be used in protein technologies including but not limited to protein or antibody arrays and enzyme-linked immunosorbent assays (ELISAs). These reagents can be used in assays or diagnostic kits to screen subjects for SLE.

Assays or diagnostic kits based on the primers and probe sets as described in Example 9 can be used with a sample from a subject with symptoms of a rheumatic disease to diagnose, classify or rule out SLE; and with a sample from a patient diagnosed with type 1 SLE or type 2 SLE to select a clinical trial, to predict flare, to detect immunosuppressant responsiveness, to determine efficacy of a therapeutic agent, to design treatment regimes, to monitor the status of the patient or treatment regime. In one alternative, the diagnostic kit includes an array of nucleic acid molecules or antibodies; in another, the diagnostic kit includes probe sets for use in quantitative RT-PCR.

Pharmacogenomics is the study of an individual's response to a particular therapeutic agent, immunosuppressant or combinations of agents. In this context, response refers to whether a particular agent or drug will work better for a particular type 1 SLE or type 2 SLE patient. The methods disclosed provide for assigning a patient to a clinical trial based on classification as type 1 SLE or type 2 SLE and disease status (quiescent or flare).

Pharmacogenomics is also important in determining the dosage of a therapeutic agent based on classification and disease status of the patient. It is contemplated that a patient diagnosed with type 1 SLE will respond differently to a particular immunosuppressant or therapeutic agent than a patient diagnosed with type 2 SLE. Individual response must also be taken into account relative to the side-effects or interactions of various immunosuppressant or therapeutic agents. Some potentially useful therapeutic agents and immunosuppressants are listed in the definitions and claims.

The present invention contains many preferred embodiments and includes material from patents, patent applications and other publications incorporated by reference in their entirety for all purposes, but especially for details in practicing the invention and known to those in the art.

EXAMPLES Example 1 Characterization of Patients and Samples

Patients who met the American College of Rheumatology (ACR) criteria for the diagnosis of SLE (malar rash, discoid rash, photosensitivity, oral ulcers, arthritis, serositis, renal disorder, neurologic disorder, hematologic disorder, immunologic disorder, and antinuclear antibody) were identified (cf. Tan et al (1982) Arthritis Rheum 25:1271-7). After institutional review and approval, patients gave informed consent and were included in the Lupus Disease Activity Monitoring and Risk Stratification Archive Discovery Microarray Study. The samples and clinical data were available via the Autoimmune Biomarkers Collaborative Network (ABCoN).

Blood and/or tissue samples and clinical data have been collected from patients managed at Johns Hopkins Medical Center (JHMC) within the Hopkins Lupus Cohort. In this cohort, all SLE patients have been followed according to protocol with visits at a minimum of every 3 months. The table below has self-explanatory columns that show demographic information for the patients in the SLE cohort.

Number (% of total cohort) Age at Entry into cohort (yrs) <30 304 (32%)  30 to 49 511 (53%)  50+ 148 (15%) Female 888 (92%) Race White 529 (55%) Black 403 (42%) Other 31 (3%) Education <12 yrs 124 (14%) High School 281 (31%) Some College 497 (55%) Years in cohort  0 191 (19%)  1 to 3 409 (41%)  4+ 391 (40%) Number of cohort visits  1 78 (8%)  2 to 8 320 (32%)  9 to 44 492 (50%)  45+ 101 (10%) Years with SLE prior to cohort entry  0 304 (31%)  1 to 4 325 (33%)  5+ 362 (36%)

As seen above, the cohort was more or less racially balanced, and its individuals represented a broad socioeconomic spectrum. The patient samples and clinical data used in this investigation were from SLE patients who had been in the cohort for more than one year. In total, these patients visited the clinic 1782 times (an average of 5.9 quarterly visits for each patient). In the alternative, samples for training and validating prediction algorithms were obtained from the Autoimmune Disease Registry of the Hospital for Special Surgery (HSS; New York City N.Y.).

Clinical data were examined for each patient in order to select samples for use in training or validation studies. Whereas additional samples can be added to the training set, a completely unique set must be used for validation. Both clinical and existing expression data were analyzed for 81 of the first 100 patients in the cohort and a subset of these patients was used for the training study. For the training study, the following classes of samples (Q=quiescent, F=flare) were defined as follows:

QF1: primary QF quiescent sample that proceeds to flare within 150 days No prior flare within 60 day 1 primary pair per patient only SLEDAI ≧4 QF4: second QF1 A second, unique QF1|F from the same patient QF4 precedes a distinct F from the QF1 Can be combined with QF1 for analysis QF5: earliest baseline additional, earlier QF for a given QF1|F F: high current disease activity SLEDAI increases ≧4 from previous visit PGA (Physician's Global Assessment) = rating of disease activity as high or increasing QQ: primary quiescent and stable SLEDAI ≦4 and no flares in next 150 days or more Sample Characteristics

The table below shows the comparison between the various classes. Column one lists the QF, F and QQ classes as defined above; column two, the groups within the class; column three, the number of patients in the class or group; column four, the average (avg) days (da) to flare; column five, the median days to flare; column six, the average (avg) increase in SLEDAI; column seven, the median (med) increase in SLEDAI; column eight, the average increase in SLEDAI at flare; and column nine, the number of visits prior to flare.

Class Group No. Avg da to F Med da to F SLEDAI avg SLEDAI med F SLEDAI Visits to F QF 1 30 87 87 5.7 4 7.6 1.1 4 3 78 84 6.7 4 8 1 5 12 227 186 F 37 7.7 QQ 34 357 340 Sample Matching

One of the most important class comparisons was QQ vs. QF. Molecular characterization of the samples that do not progress in disease activity or proceed to flare were particularly important for assessing risk and efficacy of treatment regime, determining prognosis, and the like. A typical subset of patients was characterized in the table below. In that the patients have similar clinical data, their samples showed that observed difference in class was due to activation at the molecular level (measured by gene expression) and not due to observable differences. Column one shows class or T-test; column two, number of patients (No), column three, physician's global assessment (PGA); column four, SLEDAI score, column five, prednisone treatment (Pred); column six, percent of patients on immunosuppressant treatment (Immuno); column seven, percent of patients on intravenous treatment (IVS); and column seven, percent of the patients who are female.

No PGA SLEDAI Pred Immuno IVS % Female QF1 30 0.79 1.87 6.96 47% 17% 97 QQ 34 0.58 1.65 5.33 44% 12% 88 T-test 0.14 0.60 0.41 0.84 0.58 0.22 QF1 + 4 33 0.78 1.82 7.75 45% 45% 97% QQ 34 0.58 1.65 5.33 44% 12% 88% T-test 0.17 0.68 0.26 0.91 0.69 0.18

Although none of the clinical variables was statistically significant between classes, there was a slight trend towards more severe disease in the QF group. It must be noted that this trend was not clinically relevant; and as samples are added to the study, it is expected that even this slight trend will disappear.

The normal control sample was a pooled blood sample taken from equal numbers of male and female Expression Genetics employees. These donors were healthy at the time the sample was collected, and none had obvious disease symptoms or diagnosis of SLE or any other rheumatic disease.

Example 2 Analyses of Gene Expression Profiles of SLE Patients Proceeding to Flare

The basis for diagnosing and monitoring the status of SLE in patients involved detecting differential gene expression between quiescence (QQ) and flare (QF) samples. K-means clustering of gene using GeneSpring GX 7.3 were done with the following criteria Number of clusters 15, Number of iterations 200, Similarity Measure Pearson Correlation and genes in which half of the samples did not have data were not used Genes shown in Table 1 were defined as those with a p-value≦0.05 and a fold change ≧1.2. The genes were clustered to group genes which represented a particular pathway or cell type. The table below shows the number of the cluster as presented in Table 1, the average Radius between the clusters and an all clusters average. Average Radius is calculated by the root mean square of the Euclidean distances between each gene and the centroid.

Cluster No Cell Type Average Radius 1 Granulocytes & B cells 5.15 2 NK cells 6.02 3 Granulocytes 7.23 4 Granulocytes 6.82 5 Platelet 6.31 6 All Cell Types 6.32 7 B cells 4.39 8 All Cell Types 6.85 9 B cells 5.88 10  All Cell Types 8.81 11  All Cell Types 8.34 12  All Cell Types 3.67 13  Red Blood Cells 6.87 14  Red Blood Cells 4.98 15  All Cell Types 2.19 All Clusters Ave 5.99

The genes shown in Table 1 were used with the statistical methods described below to diagnose and monitor the status of SLE patients, to predict flare and to assess treatment efficacy.

The various analyses were carried out using classification and prediction algorithms, software and programs including, but not limited to, analysis of variance, classification and regression trees (Brieman et al. (1984) Classification and Regression Trees, Wadsworth, Belmont Calif.), linear discriminatory analysis (Statsoft, Tulsa Okla.), multiple additive regression trees (Friedman (2002) Stanford University, Stanford Calif.), nearest shrunken centroids classifier (Tibshirani et al. (2002) PNAS 99:6567-6572), significance analysis of microarrays (Tusher et al. (2001) PNAS 98:5116-5121), one and two tailed T-tests, Wilcoxon's signed ranks test, and the like. The statistical analyses applied to both array and PCR expression data were also described in the Detailed Description of the Invention and in Example 5 of U.S. Pat. No. 6,905,827 incorporated by reference herein in its entirety.

In addition to expression data, any piece of clinical data collected from patients can be used in a correlation or classification analysis. Continuous variables including but not limited to albumin, autoantibodies, hemoglobin or other measures of organ function that contribute to SLEDAI score can be used for correlation analysis. In some cases, the logarithm of the values was used for the analysis. When these variables were included in the analysis, they were treated as another “gene”. For example, samples from kidney biopsies can be used to divide SLE patients into groups with or without renal disease. From the analyses of clinical manifestations carried out in this study and differences in clinical manifestations reported by others, it is contemplated that categorical variables such gender, ethnicity and socioeconomic status can also contribute to classification, prediction of flare, and selection or modulation of effective therapeutics.

Example 3 Prediction Algorithms

After all the expression and clinical data were placed in a relational database, these data were used to build prediction algorithms. The prediction algorithms were applied to gene expression profiles from SLE patients converting from quiescence to flare to identify sets of differentially expressed genes for monitoring the status of SLE, specifically for predicting flare or disease activity and effective treatment regimes.

Once a set of genes and expression criteria for those genes have been established for classification, cross-validation was done. Validation of the algorithm by these means yielded an estimate of the predictive value of the algorithm on the target population. For example, a 10-fold cross-validation analysis excluded 10% of the training samples from the analysis, and the classification algorithm was built with the remaining 90%. The 10% of the samples that were initially excluded were then used as a test set for the algorithm. The process was repeated 10 times with 10% of the samples being used as a test set each time. Through this analysis, it was possible to derive a cross-validation error which helped estimate the robustness of the algorithm for use on previously untested samples (i.e., samples that were not included in the training analysis). Untested samples came from the JHMC or HSS archives In the alternative, the samples can come from a new clinical study.

Example 4 Classification of Patients as Type 1 SLE and Type 2 SLE

Another step toward better monitoring the status of SLE patients was to classify them as having either type 1 SLE or type 2 SLE. A number of comparisons of data in the relational database were made and validated as described below.

Gene Expression Patterns

One of the comparisons of gene expression patterns was to analyze genes that were differentially expressed between paired QF1 and F samples from the same patient taken from about two to about six months apart. The first sample was from a time period when the patient's disease activity was low (SLEDAI 0-4), but the second sample from the same patient showed increased disease activity and a SLEDAI≧4. In this process, examination of some of the genes known to be expressed in inflammation or immune disorders showed nearly parallel expression patterns in paired quiescent/flare (QF) and flare (F) patient. The expression of one of those genes, IFI27, is shown in FIG. 1.

The x-axis of FIG. 1 represents patient number and the y-axis, the Log₁₀ expression ratio for IFI27, FIG. 1 demonstrates that IFI27 was not differentially expressed according to disease activity or flare. Further examination of longitudinal data showed that expression of INFr genes placed SLE patients into at least two different groups.

INFr score

The relational database of SLE data was searched for genes whose expression correlated with IFI27≧0.5 or ≦−0.5 using Pearson correlation; these designated INFr genes are listed in Table 2. Longitudinal data from an initial group of 81 patients covering a period of up to two years (including extra time points available in the QF4 and QF5 classes) was used to examine IFNr gene expression.

Although many different algorithms were contemplated, one exemplary algorithm was developed to demonstrate how to use three INFr genes to calculate an IFNr score. The genes that encode IFI27, IFI44 and OAS3, highlighted in Table 2, were used to develop the algorithm. The INFr score based on these three genes reflects the Log₁₀ ratio of patient sample expression over reference sample expression on the microarray after normalization using Feature Extraction v 7.5 software (Agilent Technologies). The standard deviation for each gene was normalized so that each of the genes would have the same influence on IFNr score. The exemplary algorithm is: IFI27+IFI144*(1.1296)+OAS3*(1.8136).

The genes used to derive INFr score are described as follows: 1) IFI27 (also known as ISG12 and p27) maps to chromosome 14q32, the location of the serine protease inhibitor gene cluster. IFI27 is induced by alpha interferon and localizes to the nuclear membrane. Since IFI27 is expressed in breast, head and neck carcinomas, it has been used to predict patient sensitivity to cisplatin and paclitaxel; 2) IFI44 (also known as MTAP44) is induced by α and β interferons, but not by γ interferon and aggregates to form microtubular-like structures in hepatitus-C infected cells; and 3) OAS3 maps to chromosome 12q24.2 and is an interferon-induced protein that catalyzes the synthesis of 2′-5′ oligomers of adenosine.

Table 3 presents longitudinal data for patients with SLE. Column one shows patient number; column two, ABCoN ID followed by sample number; column three, sample designated as quiescent (QF) or flare (F); column four, date sample taken; column five, SLEDAI score; column six, IFNr score (high or low); column seven, days from first sample; and INFr score. The cutoff for distinguishing between high IFNr and low IFNr scores was the average of all INFr scores. Table 3 demonstrated: 1) longitudinal stability of INFr score in an individual over time, 2) the existence of at least two types of SLE as defined by high and low expression of IFNr genes, and 3) lack of correlation between SLEDAI and IFNr scores as shown for patients 2, 4, 6, 9, and 15.

The change from high to low INFr score or from high to low to high INFr score as seen in the data for patients 10 and 13, respectively, were further analyzed. A Fisher's Exact Test was used to calculate a p-value for hypothesized random discordant results. The conversion of one high to low and one low to high produced the p-value=0.000034 that the events happened at random.

Another way to look at IFNr score was to compare normal control and first visit patient samples. In FIG. 2, all samples were sorted low to high and plotted according to INFr score. The normal subjects are presented on the left side of the graph, and the 81 SLE (lupus) patients are presented on the right.

The x-axis shows the number assigned each normal subject or SLE patient, and the y-axis shows INFr score where the scale is fold. As shown on this graph, INFr scores varied by as much as 500-fold. Although they appeared healthy at the time of sampling, three of the normal subjects had slightly elevated IFNr scores that were attributed to infection, allergies, or other sub-acute, non-SLE conditions.

Since the INFr scores of the SLE patients appeared as a continuous slope in the graph above, the data was parsed. The graph for IFI27, IFI44, and OAS3 (FIG. 3) clearly showed the bimodal distribution of SLE patients (type 2 SLE to the left of zero and type I SLE to the right, on the x-axis) when number of samples was graphed against log₁₀ of the expression ratio.

Similar graphs or histograms can be plotted for any of the other INFr genes shown in Table 2, and any of these INFr genes can be used to develop an algorithm to classify SLE patients as type 1 SLE or type 2 SLE.

In further support of the stability of type 1 and type 2 SLE classification, a Fisher's Exact Test was applied to the hypothesis, “Do the highs stay high and the lows stay low?” The data presented in the table below produces a p-value=8.01e-13 that further demonstrates the validity of the bimodal distribution and the presence of at least two groups, type I SLE and type 2 SLE.

First First high low Second high 48 4 Second low 4 25

Although SLEDAI scores are on average higher in type 1 SLE patients (who generally show more severe symptoms), SLEDAI did not correlate with high or low INFr score. The clinical manifestations that did associate with type 1 SLE included low serum complement levels, high anti-double stranded DNA antibodies, and more renal disease.

Example 5 Harvesting and Preparation of Blood Samples

One or more of the methods and/or procedures below were used to prepare samples from SLE patients and normal control subjects. In the first method, two tubes of blood were drawn from each patient or normal control subject using either a peripheral venous blood draw or directly from a large-bore intra-arterial or intravenous catheter inserted in the femoral artery or vein, subclavian vein or internal jugular vein. Care was taken to avoid sample contamination with heparin since it interferes with RNA preparation.

In the second method, 8 ml of blood was drawn into a VACUTAINER CPT tube (BD Biosciences (BD), San Jose Calif.) containing the anticoagulant sodium citrate, Ficoll Hypaque density fluid, and a thixotropic polyester gel barrier permeable upon centrifugation to red blood cells (RBCs) and granulocytes but not to mononuclear cells. The blood was mixed with the anticoagulant in the tube by inverting the tube 5-10 times. Then, mononuclear cells and plasma were separated using the following procedures.

In one procedure, the mononuclear cells and plasma moved to the top of the tube while the RBCs and the granulocytes were trapped beneath the gel barrier when the tube was centrifuged in a swinging bucket rotor at 1750×g for 20 min at room temperature. After, the mononuclear cells and plasma were decanted into a 15 ml tube, 5 nil of phosphate-buffered saline (PBS) were added. The tubes was inverted 5 times and centrifuged for 5 min at 1750×g to pellet the cells; the supernatant was discarded.

In a second procedure, the clear plasma layer that formed above the mononuclear cell layer during centrifugation was aspirated and discarded. Then the mononuclear cell layer was aspirated, and all of the mononuclear cells were washed from the surface of the gel barrier with PBS. Approximately 2 mls of mononuclear cell suspension were transferred to a microcentrifuge tube and centrifuged in a microcentrifuge for 3 min at 16,000 rpm to pellet the cells; the supernatant was discarded.

Following each of the methods and/or procedures above, 1.8 ml of RLT lysis buffer (Qiagen, Chatsworth Calif.) was added to the pellet, the cells and lysis buffer were pipetted up and down to ensure complete lysis. Cell lysate was frozen and stored at −80° C. until total RNA was isolated.

Example 6 RNA Preparation

RNA was prepared from the RNA samples from SLE patients or normal controls using one of the following protocols. In the first protocol: 1) samples were thawed, 2) 4 ml of chloroform were added to each tube, 3) tubes were vortexed prior to centrifugation at 2000×g for 5 min, and 5) the aqueous layer was moved to new tube and processed using the RNeasy Maxi kit (Qiagen) according to the manufacturer's instructions. RNA quality was assessed using spectrophotometry, A260/A280 spectrophotometric ratios were considered to be acceptable when they ranged between 1.6 and 2.0, and/or gel electrophoresis, when 2 μl of each sample were run on an agarose gel in the presence of ethidium bromide and no degradation of RNA and no DNA contamination were visible.

In the second protocol: 1) samples were thawed and held at room temperature for 5 min, 2) after adding 5 ml of chloroform, the samples were vortexed and incubated at room temperature for 3 min, 3) the aqueous layer was transferred to a new 50 ml tube and purified using the RNeasy Maxi kit (Qiagen), and 4) the columns were eluted twice with 1 ml RNAse free water and incubated for one min before each spin. RNAs isolated using the first and second protocols were combined when the normal control cell preparations demonstrated reproducibility. The RNAs were mixed in a 50 ml tube, aliquoted into two 15 ml storage or 1.5 ml microcentrifuge tubes (100 μl per), and stored at −80° C.

In the third protocol: total RNA was purified using the RNeasy Miniprep kit (Qiagen) according to the protocol provided. Cells were homogenized and DNAse treated on a QIASHREDDER columns (Qiagen) and purified RNA was eluted in 50 μl of water.

After the last two protocols, RNA using the Agilent 2100 bioanalyzer and RNA 6000 microfluidics chips (Agilent Technologies).

Example 7 cDNA Synthesis

cDNA was synthesized from RNA using reverse transcription with OLIGO-dT primers/random hexamers (Invitrogen, Carlsbad Calif.) at a final concentration of 0.5 ng/μl and 3 ng/μl, respectively.

For the first strand reaction, 0.5 μg of mononuclear RNA or 2 μg of whole blood RNA and 1 μl of the OLIGO-dT/random hexamers (Invitrogen) were added to water in a reaction tube to a final volume of 11.5 μl. The tube was incubated at 70° C. for 10 min, chilled on ice, centrifuged, and 88.5 μl of first strand buffer mix (Invitrogen) was added to the tube.

The first strand buffer mix contained 1×first strand buffer, 10 mM DTT (Invitrogen), 0.5 mM dATP (New England Biolabs (NEB), Beverly Mass.), 0.5 mM dGTP (NEB), 0.5 mM dTTP (NEB), 0.5 mM dCTP (NEB), 200 U of SUPERSCRIPT RNAse H reverse transcriptase (Invitrogen), and 18 U of RNAGUARD inhibitor (GE Healthcare (GEH), Piscataway N.J.). After the reaction was incubated at 42° C. for 90 min, the enzyme was heat-inactivated at 70° C. for 15 min. After adding 2 U of RNAse H (NEB) to the reaction tube, it was incubated at 37° C. for 20 min.

For second strand synthesis, 40 U of E. coli DNA polymerase (Invitrogen) and 2 U RNaseH (Invitrogen) were added to the previous reaction to bring the final volume to 150 μl Salts and nucleotides were added to a final concentration of 20 mM Tris-HCl (pH 7.0; Fisher Scientific, Pittsburgh Pa.), 90 mM KCl (Teknova, Half Moon Bay Calif.), 4.6 mM MgCl₂ (Teknova), 10 mM (NH₄)₂SO₄ (Fisher Scientific), 1×second strand buffer (Invitrogen), 0.266 mM dGTP, 0.266 mM dATP, 0.266 mM dTTP, and 0.266 mM dCTP.

After second strand synthesis for 150 min at 16° C., the cDNA was purified away from the enzymes, dNTPs, and buffers using phenol-chloroform extraction followed by ethanol precipitation in the presence of glycogen. Alternatively, the cDNA was purified on a QIAQUICK silica-gel column (Qiagen) followed by ethanol precipitation in the presence of glycogen. The cDNA was centrifuged at >10,000×g for 30 min; and after the supernatant was aspirated, the pellet was washed with 150 μl of 70% ethanol. Following recentrifugation, the supernatant was removed, and residual ethanol was evaporated at room temperature. Alternatively, the volume of column purified cDNA was reduced in a vacuum evaporator to 7.4 μl.

Example 8 Arrays

Arrays were used to produce a gene expression profile for diagnosing and monitoring the status of SLE in a patient. In one format, the array contains reagents specific for at least two genes or proteins, one that binds to a gene or protein of the invention, and one that binds to a control gene or protein.

Nucleic Acid Arrays

Human Genome CGH 44A microarrays (Agilent Technologies) were used to determine differential gene expression. These Cy₃/Cy₅ chips contained 41,675 probes (60-mers) that represented most the genes found in REFSEQ database (NCBI); additional genes on the chip represented various controls. The chips were run as recommended by the manufacturer and scanned using an Agilent DNA microarray scanner. The data was extracted using Feature Extraction v 7.5 software (Agilent Technologies).

In the alternative, Affymetrix U133A Human GeneChips (Affymetrix, Santa Clara Calif.) with probe sets representing about 14,500 full length genes and 22,000 features were used according to the manuals and product inserts supplied by the manufacturer. Affymetrix Microarray Suite (MAS) v 5.0 software was used to generate expression values for each gene. To correct for slight differences in overall chip hybridization intensity and allow for comparison between samples, each chip was scaled to an overall intensity of 1500.

In one alternative, the PAXgene Blood RNA system (PreAnalytix GmbH, Hombrechtikon Switzerland) was used for whole blood collection, stabilization, and RNA isolation from patient and/or normal samples. Five μg of total RNA was used to prepare biotinylated cRNA for hybridization using a standard protocol (Expression Analysis Technical Manual, Affymetrix). For samples with low RNA yields, two or more rounds of amplification were performed. Fifteen micrograms of each labeled cRNA was hybridized to Affymetrix U133A Human GeneChips.

In another alternative, a low density array containing amplicons produced using probe sets for genes selected from Table 1 and Table 2 are harvested from PCR reactions, purified using Sephacryl-400 beads (GEH) and arrayed on a membrane. The membrane is UV irradiated, washed in 0.2% SDS at room temperature and rinsed three times in distilled water, Non-specific binding sites on the array are blocked by incubation in 0.2% casein in PBS for 30 min at 60° C., and the arrays are washed in 0.2% SDS and rinsed in distilled water.

In another alternative, purified amplicons are robotically arranged and immobilized on polymer-coated glass slides using the procedure described in U.S. Pat. No. 5,807,522 (which is hereby incorporated in its entirety). Polymer-coated slides are prepared by cleaning glass microscope slides (Corning Life Sciences, Corning N.Y.) ultrasonically in 0.1% SDS and acetone, etching in 4% hydrofluoric acid (VWR Scientific Products, West Chester Pa.), coating with 0.05% aminopropyl silane (Sigma-Aldrich) in 95% ethanol, and curing in a 110° C. oven. The slides are washed extensively with distilled water between and after treatments.

Antibody Arrays

Monoclonal antibodies specific to at least two IFNr proteins and at least two proteins selected from the clusters of Table 1 are immobilized on a membrane, slide or dipstick or added to the wells of an ELISA plate using methods well known in the art. The array is incubated in the presence of serum or cell lysate until protein:antibody complexes are formed. The proteins encoded by genes or their splice variants are identified by the known position and labeling of the antibody that binds an epitope of that protein on the array. Quantification is normalized using the antibody:protein complex of various controls.

Example 9 Designing and Selecting Primers and Probe Sets

Primers and probe sets were designed and selected for each gene having utility in the diagnosis and monitoring of SLE using the PRIMER3 program (Whitehead Research Institute (WRI), Cambridge Mass.). Default values were used for all parameters but melting temperature (Tm). Tm was set between 71.7 and 73.7° C.; amplicon size, between 50 and 150 bases in length (optimum, about 100 bases); and primers or probes were allowed to be 36 nucleotides in length. Salt concentration, a critical parameter affecting the Tm of the probes and primers, was used at the default concentration, 50 mM.

The C source code for the PRIMER3 program was downloaded from the WRI website and complied on a Sun Enterprise 250 server (Sun Microsystems, Palo Alto Calif.) using the GCC compiler (Free Software Foundation, Boston Mass.). A subsequent version was compiled for machines running the Windows operating system (Microsoft, Redmond Wash.). The program was run from the command line which also dictated the use of an input file that contained the sequences and the parameters for primer design as described in the help files that accompanied the software. A script was written to input a number of sequences and automatically generate a number of potential primers. The following batch approach was used to design primers for the genes.

The first step in designing primers was to mask out repetitive sequences in the mRNA using the REPEATMASKER program (Institute for Systems Biology, University of Washington, Seattle Wash.). The second step was to mask out all known SNPs for the genes as annotated in the SNP database at NCBI (Bethesda Md.) that have an allelic heterozygosity higher than 1%. The masked sequence was submitted to PRIMER3 using parameters as outlined above, and the top eight sequences were selected. Alternatively, the Primer3 program was used on the MIT website (Massachusetts Institute of Technology, Cambridge Mass.) to examine a specific region on the mRNA of a particular gene. The final step was to test several of the top pairs of primers for correct size and efficiency.

Primers were ordered from Integrated DNA Technologies (Coralville Iowa) or an alternative commercial source.

Example 10 Testing of Primers and Probe Sets for RT-PCR

Control genes: With both microarrays and RT-PCR, variation was monitored by adding one or more genes from bacteria, plants, or animals in one or more wells. Although human β-actin and β-GUS were used to validate the control RNAs, several other genes were also tested for variability between samples, for expression in mononuclear and whole blood RNA from control subjects and SLE patients, on samples prepared using various protocols, and in the RT-PCR assays.

Based on criteria of low variability between control and patient samples and high expression across samples, β-actin, β-GUS, 18s ribosomal subunit, GAPDH, and β2-microglobulin were selected as the control genes and used in the various assays.

Primer Testing: Primers were tested once using RT-PCR protocol (without Rox and Sybr green dyes) to see whether they produced an amplicon of the correct size without amplifying non-specific sequences. Each primer pair/probe set was tested on cDNA made from mononuclear cell control RNA described in Example 2. The PCR reaction contained 1×RealTime-PCR buffer (Ambion, Austin Tex.), 2 mM MgCl₂ (ABI), 0.2 mM dATP (NEB), 0.2 mM dTTP (NEB), 0.2 mM dCTP (NEB), 0.2 mM dGTP (NEB), 0.625 U AMPLITAQ Gold enzyme (ABI), 0.3 μM of each primer to be used (Sigma Genosys, The Woodlands Tex.), 5 μl of the reverse transcription reaction, and water added to a final volume of 19 μl.

Following 40 cycles of PCR, 101 of each product were combined with Sybr Green dye at a final dilution of 1:72,000. Melt curves for each PCR product were determined on a PRISM 7900HT Sequence detection system (ABI), and primer pairs yielding a product with one clean peak were chosen for further analysis. One μl of product from each probe set assay was examined by agarose gel electrophoresis or using a DNA 1000 chip kit and an Agilent 2100 bioanalyzer (Agilent Technologies). From primer design and the genomic sequence, the expected size of the amplicon was known. Only primer pairs showing amplification of the single desired product, and minimal amplification of contaminants, were used in assays.

Primers were tested a second time to determine their efficiency in an RT-PCR reactions. cDNA was synthesized as described above. A set of 5 serial dilutions of cDNA in water: 1:10, 1:20, 1:40, 1:80, and 1:160 was tested using RT-PCR.

Example 11 RT-PCR Assays and Analysis

TAQMAN: PCR reactions were performed using the TAQMAN Universal PCR Master mix (ABI). The master mix was aliquoted into light tight tubes, one for each gene. The primer pair for each gene was added to the tube of PCR master mix labeled for that gene. A FAM/TAMRA dual labeled TAQMAN probe (Biosearch Technologies, Novato Calif.) was added to each tube. Alternatively, different combinations of commercially available fluorescent reporter dyes and quenchers were used such that the absorption wavelength for the quencher matches the emission wavelength for the reporter.

In one alternative, a Sybr green RT-PCR reaction can be performed using the TAQMAN PCR reagent kit (ABI). In the alternative, Universal ProbeLibrary (LNAs; Roche Diagnostics, Pleasanton Calif.), were substituted for Taqman probes.

RT-PCR Assays and Analysis: 18 μl of master mix were dispensed into each well of a 384 well plate (ABI), and 2 μl of the template sample were dispensed into triplicate wells for each primer pair. The final concentration of each reagent was: 1×TAQMAN Universal PCR Master Mix, 300 nM each primer, 0.25 nM TAQMAN probe, and 21 μl of 1:10 diluted template. PCR reactions were run on the PRISM 7900HT Sequence Detection system (ABI) with the following conditions: 10 min at 95° C.; 40 cycles of 95° C. for 15 sec, 60° C. for 1 min.

Sequence detection system v2.0 software (ABI) was used to analyze the fluorescent signal from each reaction. Standard deviation (Stdev) and coefficient of variation (CV) were calculated for triplicate wells. If the CV was greater than 2, an outlier among the three wells was identified and deleted; and the average was recalculated. In each plate, the difference in CT (ΔCT) was calculated for each gene and control combination by subtracting the average CT of the gene from the average CT of the control. The expression relative to the control was calculated by taking two to the power of the ΔCT of the gene.

In each case, all plates were run in duplicate and analyzed in the same manner. The percent variation was determined for each sample and gene combination (relative expression, RE) by taking the absolute value of the RE for the second plate from the RE for the first plate, and dividing that by the average. If more than a quarter of the variation calculations on a plate were greater than 50%, then a third plate was run. The cycle number at which each amplification curve crossed CT was recorded, and the file was transferred to MS Excel for further analysis. CT values for triplicate wells were averaged, and data were plotted as a function of the log₁₀ of the calculated starting concentration of RNA. The starting RNA concentration for each cDNA dilution was determined based on the original amount of RNA used in the reverse transcription reaction, the dilution of the reverse transcription reaction, and the amount used in the RT-PCR reaction (usually 5 μl). For each gene, a linear regression line was plotted through all points of the dilution series. The slope of the line was used to calculate efficiency of the reaction for each primer set using the equation, E=10^((−1/slope))−1. This efficiency equation was used to compare the expression of primers or probe sets for each gene, and a primer pair was considered successful if the efficiency was reproducibly determined to be 0.85-1.2.

Since variation of RT-PCR assays can arise from unequal amounts of RNA starting material, probe sets for control genes can be run in the same reaction as the probe set for the diagnostic gene to reduce variation. Different fluorescent dyes were used to amplify the control, differentiating their expression from that of the diagnostic gene.

Quantitative RT-PCR: RT-PCR was used to compare the expression of each gene using the primers described above. cDNA was synthesized from normal control, patient, and reference samples. Ten μl RT-PCR reactions were performed using a PRISM 7900 Sequence Detection system (ABI) using FAM-TAMRA labeled probes and the standard TAQMAN protocols described above. RT-PCR amplification product was measured as CT (threshold cycle=the point at which an amplification curve crosses a threshold fluorescence value) during the PCR reaction to observe amplification before any reagent became rate limiting. Threshold was set to a point where all of the reactions were in their linear phase of amplification. A lower CT indicated a higher amount of starting material (greater expression in the sample) since an earlier cycle number meant the threshold was crossed more quickly. A CT of less than 30 based on appropriate cDNA dilutions provided linear results for the blood samples from SLE patients.

In the alternative, other labeling moieties or technologies can be used to measure amplification product in RT-PCR. Molecular beacons (Invitrogen) use FRET technology, and fluorescence is measured when a hairpin structure is relaxed by the specific probe binding to the amplicon.

Other labeling moieties can be used for detection of an antibody, nucleic acid or protein in any of the assays or diagnostic kits described herein. These labeling moieties include fluorescent, chemiluminescent, or chromogenic agents, cofactors, enzymes, inhibitors, magnetic particles, radionuclides, reporters/quenchers, substrates and the like that can be attached to or incorporated into the antibody, nucleic acid or protein. Visible labels and dyes include but are not limited to anthocyanins, avidin-biotin, β glucuronidase, biotin, BIODIPY, Coomassie blue, Cy3 and Cy5, 4,6-diamidino-2-phenylindole (DAPI), digoxigenin, ethidium bromide, FAM/TAMRA, FITC, fluorescein, gold, green fluorescent protein, horseradish peroxidase, lissamine, luciferase, phycoerythrin, reporter/quencher pairs (HEX/TAMRA, JOE/TAMRA, ROX/BHQ2, TAMRA/BHQ2, TET/BHQ1, VIC/BHQ1, and the like), rhodamine, spyro red, silver, streptavidin, and the like. Radioactive markers include radioactive forms of hydrogen, iodine, phosphorous, sulfur, and the like.

Example 12 Protein Expression

Adapter sequences for subcloning are added at either end of a coding region specific to a gene or a portion thereof and amplified using PCR. An epitope or affinity tag (6×his) or sequences for secretion from a cell can be added to the adapter sequence to facilitate purification and/or detection of the protein. The amplified cDNA is inserted into a shuttle or expression vector that can replicate in bacteria, insect, yeast, plant, or mammalian cells. Such vectors typically contain a promoter that operably links to the coding region, replication start sites, and antibiotic resistance or metabolite selection sequences.

The expression vector can be used in an in vitro translation system or to transfect cells. For example, Spodoptera frugiperda (Sf9) insect cells are infected with recombinant Autographica californica nuclear polyhedrosis virus (baculovirus). The polyhedrin gene is replaced with the cDNA by homologous recombination, and the polyhedrin promoter drives transcription. The protein is synthesized as a fusion protein with an affinity tag that enables purification.

Clones of transformed cells are analyzed to ensure that the inserted sequence is expressed. Once expression is verified, the cells are grown under selective conditions; and the protein is isolated from cells, or if secreted, from the growth media using chromatography, size exclusion chromatography, immunoaffinity chromatography, or other methods including cell fractionation, ion exchange, or selective precipitation.

The isolated and purified protein is then used as a reagent on an array or as an antigen to produce specific antibodies.

Example 13 Antibody Production and Testing

If antibodies are to be used as reagents, the sequence of the gene or splice variant is analyzed to determine regions of high immunogenicity (LASERGENE software; DNASTAR, Madison Wis.), and an appropriate oligopeptide is synthesized and conjugated to keyhole lympet hemocyanin (KLH; Sigma-Aldrich, St Louis Mo.).

Immunization

Rabbits are injected with the oligopeptide-KLH complexes in complete Freund's adjuvant, and the resulting antisera is tested for specific recognition of the protein or fragments thereof. Antisera that react positively with the protein are affinity purified on a column containing beaded agarose resin to which the synthetic oligopeptide has been conjugated (SULFOLINK kit; Pierce Chemical, Rockford Ill.). The column is equilibrated using 12 ml IMMUNOPURE Gentle Binding buffer (Pierce Chemical). Three ml of rabbit antisera is combined with one ml of binding buffer and poured into the column. The column is capped (on the top and bottom), and antisera is allowed to bind with the oligopeptide by gentle shaking at room temperature for 30 min. The column is allowed to settle for 30 min, drained by gravity flow, and washed with 16 ml binding buffer (4×4 ml additions of buffer). The antibody is eluted in one ml fractions with IMMUNOPURE Gentle Elution buffer (Pierce Chemical), and absorbance at 280 nm is determined. Peak fractions are pooled and dialyzed against 50 mM Tris, pH 7.4, 100 mM NaCl, and 10% glycerol. After dialysis, the concentration of the purified antibody is determined using the BCA assay (Pierce Chemical), aliquoted, and frozen.

Electrophoresis and Blotting

Samples containing protein are mixed in 2×loading buffer, heated to 95° C. for 3-5 min, and loaded on 4-12% NUPAGE Bis-Tris precast gel (Invitrogen). Unless indicated, equal amounts of total protein are loaded into each well. The gel is electrophoresed in 1×MES or MOPS running buffer (Invitrogen) at 200 V for approximately 45 min on an XCELL II apparatus (Invitrogen) until the RAINBOW marker (GEH) resolves and the dye front approaches the bottom of the gel. The gel is soaked in 1×transfer buffer (Invitrogen) with 10% methanol for a few minutes; and a PVDF membrane (Millipore, Billerica Mass.) is soaked in 100% methanol for a few seconds to activate it. The membrane, the gel, and supports are placed on the TRANSBLOT SD transfer apparatus (Biorad, Hercules Calif.) and a constant current of 350 mA is applied for 90 min.

Conjugation with Antibody and Visualization

After the proteins are transferred to the membrane, it is blocked in 5% (w/v) non-fat dry milk in 1×phosphate buffered saline (PBS) with 0.1% Tween 20 detergent (blocking buffer) on a rotary shaker for at least 1 hr at room temperature or at 4° C. overnight. After blocking, the buffer is removed, and 10 ml of primary antibody in blocking buffer is added and incubated on the rotary shaker for 1 hr at room temperature or overnight at 4° C. The membrane is washed 3 times for 10 min each with PBS-Tween (PBST), and secondary antibody, conjugated to horseradish peroxidase, is added at a 1:3000 dilution in 10 ml blocking buffer. The membrane and solution are shaken for 30 min at room temperature and washed three times for 10 min with PBST.

The wash solution is carefully removed, and the membrane is moistened with ECL+chemiluminescent detection system (GEH) and incubated for approximately 5 min. The membrane, protein side down, is placed on x-ray film (Eastman Kodak, Rochester N.Y.) and developed for approximately 30 seconds. Antibody:protein complexes are visualized and/or scanned and quantified.

TABLE 1 Ratio cell type Clus- to all ter cells cell Type Array ID Genbank ID Gene ID Description Sequence 1 Granulocytes and B cells 1 A_23_P113258 NM_005739 RASGRP1 Homo sapiens RAS guanyl releasing protein 1 AGAAGAAAATAGAATCCCTCCAGCTTGAAAAA (calcium and DAG-regulated) (RASGRP1), mRNA AGCAATCATGTCTTAGCTCAAATGGAGC (SEQ ID NO: 1) 1 A_23_P117599 NM_012111 AHSA1 Homo sapiens AHA1, activator of heat shock ATTAGTGTGAGCCTTGCCAAAGATGAGCCTGA 90 kDa protein ATPase homolog 1 (yeast) CACAAATCTCGTGGCCTTAATGAAGGAA (SEQ (AHSA1), mRNA ID NO: 2) 1 A_23_P128230 NM_002135 NR4A1 Homo sapiens nuclear receptor subfamily 4, group AATGACAGATTCTGACATTTATATTTGTGTATTT A, member 1 (NR4A1), transcript variant 1, mRNA TCCTGGATTTATAGTATGTGACTTTT (SEQ ID NO: 3) 1 A_23_P134078 NM_004824 CDYL Homo sapiens chromodomain protein, Y-like AGGTACAGATACCTCAGATTCGGGAAACTCAA (CDYL), transcript variant 1, mRNA AATCAAAAGACTTAGCTTCTAGGATAAA (SEQ ID NO: 4) 1 A_23_P251686 NM_005160 ADRBK2 Homo sapiens adrenergic, beta, receptor kinase 2 GTCAAAATGGGTTAACTGTGTATATTGACTTTC (ADRBK2), mRNA ATGTCGTCATGCATCTGTCATGAATGA (SEQ ID NO: 5) 1 A_23_P43580 NM_007018 CEP1 Homo sapiens centrosomal protein 1 (CEP1), AACCTAGAAGGAGAATTGGAAAGCTTGAAAGA mRNA GAACCTTCCATTTACCATGAATGAGGGA (SEQ ID NO: 6) 1 A_23_P46781 NM_003638 ITGA8 Homo sapiens integrin, alpha 8 (ITGA8), mRNA CCCATTATGGGTAATAATACTAGCAATACTTCT TGGATTGTTGGTTCTCGCCATTTTAAC (SEQ ID NO: 7) 1 A_23_P54170 NM_005466 MED6 Homo sapiens mediator of RNA polymerase II AGGCACCAGACTTGGGATCAGTTATAAACTCT transcription, subunit 6 homolog (yeast) (MED6), AGAGTGCTTACTGCAGTGCATGGTATTC (SEQ mRNA ID NO: 8) 1 A_23_P64689 NM_014871 USP52 Homo sapiens ubiquitin specific peptidase 52 CCAGATGGAAAGTAATTGGTATTCTTAATATCC (USP52), mRNA TGGGTGACTAATATCCAGGCAGAGAAG (SEQ ID NO: 9) 1 3 Granulocyte A_24_P115932 NM_004778 GPR44 Homo sapiens G protein-coupled receptor 44 TGGATGAAATGTCAGTGGAAGAAGCAGATGAG (GPR44), mRNA AAACTCTTGAGATCTTGGTCCTGTGTTT (SEQ ID NO: 10) 1 A_24_P227585 NM_018559 KIAA1704 Homo sapiens KIAA1704 (KIAA1704), mRNA TGATGACACATCTGGAGATCGATCAATCTGGA CAGATACTCCAGCTGATAGGGAAAGGAA (SEQ ID NO: 11) 1 A_24_P229658 GAAGGGCGTAGTCACAGAACTCGAAGTAGGA GCCGAGATAAATCCCATAGGCATAAAAAA (SEQ ID NO: 12) 1 A_24_P312692 NM_006595 API5 Homo sapiens apoptosis inhibitor 5 (API5), mRNA TTGCTATTCAAATCAACTGCCTGAATGACATTT CTAGTAGTCTGATGTATTTTTCTGAGG (SEQ ID NO: 13) 1 A_24_P341489 AC003043 Homo sapiens chromosome 17, clone ATCTGAAGTCTGTCCAGGAACTCATTTTGAAAC HRPC1067M6, complete sequence. ATGGACAAGCCAAGATAAGGAATAAGA (SEQ ID NO: 14) 1 3 B cells A_24_P359165 AC026250 Homo sapiens chromosome 11, clone RP11- TGGATAATTGAAGCCAGTGGTTTTTTAACCAAT 540A21, complete sequence. GTTATGTATCAGAATCACCTCACAAAG (SEQ ID NO: 15) 1 A_24_P4426 NM_014937 INPP5F Homo sapiens inositol polyphosphate-5- TCTCATTTGATCCTAATTTTCCCCGTATTCTAC phosphatase F (INPP5F), transcript variant 1, TTGAACACATTAAAAATACTCTGCTGC (SEQ ID mRNA NO: 16) 1 A_24_P8140 AK124166 Homo sapiens cDNA FLJ42172 fis, clone AGCTACTTAGGGTGAGCCTGCCTTCTTCCATT THYMU2029676. CTATCCGAAGTCTCTTCTAAAGTTGCGG (SEQ ID NO: 17) 1 A_24_P861009 NM_001007246 BRWD1 Homo sapiens bromodomain and WD repeat AGTCACAGATCCTACGTATGTGCTCTTCAGTA domain containing 1 (BRWD1), transcript variant GAGGATTTTCTGTGATCCTACAATGAAG (SEQ 3, mRNA ID NO: 18) 1 A_24_P865672 AC018347 Homo sapiens chromosome 15 clone RP11- AAAGCACCGGTGAAGAAATCTATAAAGATGCT 410F2, complete sequence. CCAGCCGAAAATGCACAGAAGTCAAATC (SEQ ID NO: 19) 1 A_32_P90551 NM_014230 SRP68 Homo sapiens signal recognition particle 68 kDa GACTTACATCAAGCTGTCAATGGCAATCAAGC (SRP68), mRNA GTAATGAGAGCATGGCCAAAGGTCTGCA (SEQ ID NO: 20) 1 A_32_P98683 AC006449 Homo sapiens chromosome 17, clone TGAGGGGTGCCTTCATTCCCCTTTGTTCACTT hCIT.58_E_17, complete sequence. TCTCCAGCTCAACTTGGGACTTGGGTGG (SEQ ID NO: 21) 2 NK cells 2 A_23_P10025 NM_006159 NELL2 Homo sapiens NEL-like 2 (chicken) (NELL2), ACATCACCATGTAGAAGAATGGGCGTACAGTA mRNA TATACCGTGACATCCTGAACCCTGGATA (SEQ ID NO: 22) 2 A_23_P103765 NM_002001 FCER1A Homo sapiens Fc fragment of IgE, high affinity I, AGCTCCGCGTGAGAAGTACTGGCTACAATTTT receptor for, alpha polypeptide (FCER1A), mRNA TTATCCCATTGTTGGTGGTGATTCTGTT (SEQ ID NO: 23) 2 A_23_P103775 NM_032270 LRRC8C Homo sapiens leucine rich repeat containing 8 AAACTCTGAAGATTGGAAAAAACAGCCTATCT family, member C (LRRC8C), mRNA GTACTTTCACCGAAAATTGGAAATTTGC (SEQ ID NO: 24) 2 A_23_P107283 NM_002145 HOXB2 Homo sapiens homeo box B2 (HOXB2), mRNA ATTAAACTCTAGGGGGACTTTCTTAAAAATAAC TAGAGGGACCTATTTTCCTCTTTTTTA (SEQ ID NO: 25) 2 A_23_P117662 NM_002112 HDC Homo sapiens histidine decarboxylase (HDC), CCGAGGGTAGACAGGCAGCTTCTGTGGTTCA mRNA GCTTGTGACATGATATATAACACAGAAAT (SEQ ID NO: 26) 2 A_23_P119418 NM_003796 C19orf2 Homo sapiens chromosome 19 open reading TCGCAAATCCATCCTGAAGTCTCGAAGTAGAG frame 2 (C19orf2), transcript variant 1, mRNA AGAATAGTGTGTGTAGCGACACTAGTGA (SEQ ID NO: 27) 2 A_23_P12572 NM_001227 CASP7 Homo sapiens caspase 7, apoptosis-related AGTTCTATAAGTGAGGAAGAGTTTATGGCAAA cysteine peptidase (CASP7), transcript variant GATTTTTGGGACTTTGTTTTCAAGATGG (SEQ alpha, mRNA ID NO: 28) 2 A_23_P126057 NM_001007099 SCP2 Homo sapiens sterol carrier protein 2 (SCP2), ACATTGGCAAATAGCGTGGGATAGATTTGTTT transcript variant 3, mRNA CTTAATGGGTGTGACCAATCCTGTTTTT (SEQ ID NO: 29) 2 A_23_P127676 NM_014633 CTR9 Homo sapiens SH2 domain binding protein 1 TAAACCCAGATGCTAAATCATTCCTACAAAGGT (tetratricopeptide repeat containing) (SH2BP1), TTGACTGAAACTGTGGCAGATGTCTCA (SEQ mRNA ID NO: 30) 2 A_23_P129128 NM_152334 TARSL2 Homo sapiens threonyl-tRNA synthetase-like 2 TGACCCTTAAAAATGTATTTTTCTTAACATGTTA (TARSL2), mRNA GTACTTCTACGACTTTGGAGCCACTG (SEQ ID NO: 31) 2 A_23_P133543 NM_017415 KLHL3 Homo sapiens kelch-like 3 (Drosophila) (KLHL3), TGGCTGTTAGGGACTGTATATCTTGTAAAAGA mRNA ACACTTGTCACATGCTTGATCAGTTACA (SEQ ID NO: 32) 2 A_23_P135857 NM_004836 EIF2AK3 Homo sapiens eukaryotic translation initiation CCTCCAATAAAGGGAAAATGAAGCTTTTTATGT factor 2-alpha kinase 3 (EIF2AK3), mRNA AAATTGGTTGAAAGGTCTAGTTTTGGG (SEQ ID NO: 33) 2 A_23_P14543 NM_006020 ALKBH Homo sapiens alkB, alkylation repair TTGGCTGTAATGTATGTTGAGAAGTCAGTCCA homolog (E. coli) AGGAGGTATGTTCTTCCACAACAGCCTT (SEQ (ALKBH), mRNA ID NO: 34) 2 A_23_P14804 NM_005724 TSPAN3 Homo sapiens tetraspanin 3 (TSPAN3), transcript GGCTTTATAGGAGGAGTATAATGTATGCACTA variant 1, mRNA CTGTTTTAAAAGAATTAGTGTGAGTGTG (SEQ ID NO: 35) 2 A_23_P152353 NM_133451 KIAA1970 Homo sapiens KIAA1970 protein (KIAA1970), TGGCCAATCTTGTCTGAGTTCTTTGATGGCGA mRNA CACATGAACTACAGCCGTTTTGTTGTTG (SEQ ID NO: 36) 2 A_23_P200015 NM_012093 AK5 Homo sapiens adenylate kinase 5 (AK5), transcript AATGCAGAGGGAACACCAGAGGACGTTTTTCT variant 2, mRNA TCAACTCTGCACAGCTATTGACTCTATT (SEQ ID NO: 37) 2 A_23_P208477 NM_001419 ELAVL1 Homo sapiens ELAV (embryonic lethal, abnormal GGAGGCGTAAAATGGCTCTGTATTTTAATAAC vision, Drosophila)-like 1 (Hu antigen R) ACAGAAACATTTGAGCATTGTATTTCTC (SEQ (ELAVL1), mRNA ID NO: 38) 2 A_23_P213045 NM_016269 LEF1 Homo sapiens lymphoid enhancer-binding factor 1 AGCAGGAGCCAAAAAGACCTCACATTAAGAAG (LEF1), mRNA CCTCTGAATGCTTTTATGTTATACATGA (SEQ ID NO: 39) 2 A_23_P214882 NM_019041 MTRF1L Homo sapiens mitochondrial translational release CATAAAGTCAAAAAATCCTAAAACATAAGTTGG factor 1-like (MTRF1L), mRNA TGACCATCTGTAATCATGATGTGGTGG (SEQ ID NO: 40) 2 A_23_P215566 NM_001621 AHR Homo sapiens aryl hydrocarbon receptor (AHR), AATGGCTTCGGACAAAATATCTCTGAGTTCTGT mRNA GTATTTTCAGTCAAAACTTTAAACCTG (SEQ ID NO: 41) 2 A_23_P215956 NM_002467 MYC Homo sapiens v-myc myelocytomatosis viral TTCAAATGCATGATCAAATGCAACCTCACAACC oncogene homolog (avian) (MYC), mRNA TTGGCTGAGTCTTGAGACTGAAAGATT (SEQ ID NO: 42) 2 A_23_P217187 HS333E23 Human DNA sequence from clone RP3-333E23 on TTTTTCTAACAGGCAAGACAGTGTGAAGAATT chromosome Xq21.1 Contains the P2RY10 gene GAAGCAATATGTGCATAAATTTCAGGAC (SEQ for purinergic receptor P2Y G-protein coupled 10, ID NO: 43) complete sequence. 2 A_23_P25566 NM_004951 EBI2 Homo sapiens Epstein-Barr virus induced gene 2 CTGAAACGGCAAGTCAGTGTATCGATTTCTAG (lymphocyte-specific G protein-coupled receptor) TGCTGTGAAGTCAGCCCCTGAAGAAAAT (SEQ (EBI2), mRNA ID NO: 44) 2 3 NK A_23_P302018 NM_003328 TXK Homo sapiens TXK tyrosine kinase (TXK), mRNA GCTGAGAGTGCTTCCTTCTTGAAGACGAGTGT CATTCATCACTTCAGTGATCCATGCATA (SEQ ID NO: 45) 2 A_23_P31376 NM_018334 LRRN3 Homo sapiens leucine rich repeat neuronal 3 GCCTCTCTCCAGAAATGAACTGTGATGGTGGA (LRRN3), mRNA CACAGCTATGTGAGGAATTACTTACAGA (SEQ ID NO: 46) 2 A_23_P33643 XM_937367 IL7R PREDICTED: Homo sapiens interleukin 7 receptor GCAATGAGTGAACTGACTGTGGCTACATTCTT (IL7R), mRNA GAAGATATACGGGAGAGACGTATTATTA (SEQ ID NO: 47) 2 A_23_P338919 NM_005876 APEG1 Homo sapiens aortic preferentially expressed gene GCAGGGGGCCACTGTAGTGAGCGTGGAGAAA 1 (APEG1), mRNA TTTGGAAACACCTATTTCTTAACTCAAAT (SEQ ID NO: 48) 2 A_23_P343398 NM_001838 CCR7 Homo sapiens chemokine (C-C motif) receptor 7 AAGAGAGCAACATTTTACCCACACACAGATAA (CCR7), mRNA AGTTTTCCCTTGAGGAAACAACAGCTTT (SEQ ID NO: 49) 2 A_23_P345460 NM_015432 PLEKHG4 Homo sapiens pleckstrin homology domain GACTTGATGCCTTTTGAATAACTTTCAATAGAA containing, family G (with RhoGef domain) TTGTCTAAAATTATCTTACTGGTTGTT (SEQ ID member 4 (PLEKHG4), mRNA NO: 50) 2 A_23_P354151 NM_005546 ITK Homo sapiens IL2-inducible T-cell kinase (ITK), TTGAACACTTCATGAGGAGGGACATTCCCTGA mRNA TATAAGAGAGGATGGTGTTGCAATTGGC (SEQ ID NO: 51) 2 A_23_P384085 NM_014635 GCC2 Homo sapiens GRIP and coiled-coil domain TCTCTTAAGCCTTCAGTTTATACTCTTAATTTAA containing 2 (GCC2), transcript variant 2, mRNA TTTTCTTTCTGAGCTGGAGAACTGGC (SEQ ID NO: 52) 2 A_23_P404481 NM_001400 EDG1 Homo sapiens endothelial differentiation, GCTGAGGCCAAAGTTTCCATGTAAGCGGGATC sphingolipid G-protein-coupled receptor, 1 CGTTTTTTGGAATTTGGTTGAAGTCACT (SEQ (EDG1), mRNA ID NO: 53) 2 A_23_P436117 NM_018200 HMG20A Homo sapiens high-mobility group 20A (HMG20A), CACTTGACAGTGACTTGAAACATTTGCATATTC mRNA AGGAATGCATGAGATTTCAAGAGAGCC (SEQ ID NO: 54) 2 A_23_P45726 NM_005826 HNRPR Homo sapiens heterogeneous nuclear GGGATAGATTACATAGGAGTATGGAGTATGCT ribonucleoprotein R (HNRPR), mRNA GTAAATAAAAATACAAGCTAGTGCTTTG (SEQ ID NO: 55) 2 A_23_P55682 NM_023926 ZNF447 Homo sapiens zinc finger protein 447 (ZNF447), GCAAGTGGTCACCAGCATTACACAGCAATGAA mRNA GCAGAATAAAGTAGGCCAGAATGCATCA (SEQ ID NO: 56) 2 A_23_P68198 NM_015677 SH3YL1 Homo sapiens SH3 domain containing, Ysc84-like TGGAGACAGAATCACAGTTATATCAAAAACAG 1 (S. cerevisiae) (SH3YL1), mRNA ATTCACATTTTGATTGGTGGGAAGGAAA (SEQ ID NO: 57) 2 A_23_P78268 NM_016080 C17orf25 Homo sapiens chromosome 17 open reading TAATCCCGACAGAACATCATGTGAGATTTCTTT frame 25 (C17orf25), mRNA AAAATGGATTAAACGATTTCTTCAGCC (SEQ ID NO: 58) 2 A_23_P83931 NM_005863 NET1 Homo sapiens neuroepithelial cell transforming TCTTTGAAAGGGGGGAGGAGGAGTAAAAGCC gene 1 (NET1), mRNA CGATTATAATGGTGATCAATTCAAGTCAG (SEQ ID NO: 59) 2 A_23_P91991 NM_138381 MGC15763 Homo sapiens hypothetical protein BC008322 ATGTACCCAAAGAACACATTTGCTTTGAGAAGT (MGC15763), mRNA GGTGGTAGGAGGCAGACAAAGGCAGAA (SEQ ID NO: 60) 2 A_23_P94889 AC103817 Homo sapiens chromosome 8, clone CTD- TAAGTTTTGTAAAAAGGAGCATCTTGAATCCAC 3083F21, complete sequence. TTAGATAAAGACAGACTGTGTGTGTAG (SEQ ID NO: 61) 2 A_24_P108291 NM_018439 IMPACT Homo sapiens Impact homolog (mouse) AGAGCCTTTCTGAAGAGAATTATATCAAACTAA (IMPACT), mRNA TTACAACCAAGAAATAATAGTATGAAG (SEQ ID NO: 62) 2 A_24_P117528 NM_002765 PRPS2 mRNA CAAGGCCTAAAGCCAACTGACTTAAAGGTAAT CATTTCAGCTAAGATTAAATTTAAAGCC (SEQ ID NO: 63) 2 A_24_P12521 NM_138811 C7orf31 Homo sapiens chromosome 7 open reading frame GGTGCACAAAAGCGTTTCCATAAATCAATTCTA 31 (C7orf31), mRNA GAAGACCATAAAGACCTCAGGGATAAT (SEQ ID NO: 64) 2 A_24_P136438 NM_014915 ANKRD26 Homo sapiens ankyrin repeat domain 26 ATGTTGATGAAGTGCACAAAAATAATAGAAGTG (ANKRD26), mRNA ATATGATGTCCGCATTAGGATTAGGAC (SEQ ID NO: 65) 2 A_24_P157424 NM_007362 NCBP2 Homo sapiens nuclear cap binding protein subunit CCCGTTAAACTGAGTGTAGAAATCTGAATTTTT 2, 20 kDA (NCBP2), mRNA AAAAGAGCTGTAACTAGTTGTAAGTGC (SEQ ID NO: 66) 2 A_24_P16361 ACCAAAAAATTCATGAGAGATCCAATTAATTCT GGTGAAAAAGGATTGACCCTTGAAGGA (SEQ ID NO: 67) 2 A_24_P170103 AACGACAACAGAAAAACAATCTTATTCCAAGTC ATTCCAGTAACTTTTTTGGGTACGTAC (SEQ ID NO: 68) 2 A_24_P170186 AL589796 Human DNA sequence from clone RP13-469O16 ATGCACAAAAGTCAAATCAGAATGGAGACTCA on chromosome 6 Contains a nucleophosmin AAACCATCAAAGCTAAGATCAAAAGGTC (SEQ (nucleolar phosphoprotein B23, numatrin) ID NO: 69) (NPM1)(B23, NPM) pseudogene and a CpG island, complete sequence. 2 A_24_P202555 NM_015073 SIPA1L3 Homo sapiens signal-induced proliferation- TGCAAAAACAGATCTATTTAATTTGAGGTTGAT associated 1 like 3 (SIPA1L3), mRNA GTTCTATCCAATGGCCGAAGATAGCAG (SEQ ID NO: 70) 2 A_24_P208345 NM_033102 SLC45A3 Homo sapiens solute carrier family 45, member 3 GTGCCGTTTGCAATAATGTCGTCTTATTTATTT (SLC45A3), mRNA AGCGGGGTGAATATTTTATACTGTAAG (SEQ ID NO: 71) 2 A_24_P212596 AC019288 Homo sapiens chromosome 15, clone RP11- TTTTCAACAGTACAGAAAAATTGAAAAAAGGGG 139F4, complete sequence. CTTTGCCTTTGTAACCTTTGATGACCA (SEQ ID NO: 72) 2 A_24_P218970 NM_001417 EIF4B Homo sapiens eukaryotic translation initiation TTTTTAAGCTTCCCTTGAGAGAATAAATGGTAA factor 4B (EIF4B), mRNA TGGAGAGAACTATTTAACAAGGTCCTG (SEQ ID NO: 73) 2 A_24_P234921 NM_004367 CCR6 Homo sapiens chemokine (C-C motif) receptor 6 AAGCTTTAACTATATCTCTCTTTAAAATGCAAAA (CCR6), transcript variant 1, mRNA TAATGTCTTAAGATTCAAAGTCTGTA (SEQ ID NO: 74) 2 A_24_P251381 NM_024782 XLF Homo sapiens XRCC4-like factor (XLF), mRNA ACCTTGAAAGAAGCTTACATGGCAGCAATATTT CTAAAATAGTGATACAGTCAGAGGCCT (SEQ ID NO: 75) 2 A_24_P26073 NM_133259 LRPPRC Homo sapiens leucine-rich PPR-motif containing AGAGAAAGATGTCACATCTGCTAAAGCACTGT (LRPPRC), mRNA ATGAACATTTGACTGCAAAGAATACAAA (SEQ ID NO: 76) 2 A_24_P299911 NM_015148 PASK Homo sapiens PAS domain containing ATCTTGCTGACTATACATGGGAAGAGGTGTTT serine/threonine kinase (PASK), mRNA CGAGTAAACAAGCCAGAAAGTGGAGAGTTC (SEQ ID NO: 77) 2 A_24_P302506 AL355145 Human DNA sequence from clone RP5-831G13 AATTGGAGAATTGAATAATCAGCATATGTAAGC on chromosome 1 GCACTAGAACCCTGTGTTGAAAACTGC (SEQ ID NO: 78) 2 A_24_P307384 XM_927265 LOC643288 PREDICTED: Homo sapiens similar to 60 kDa CTAGTGAATATGAAAAGGAAAAACTGAATGAA heat shock protein, mitochondrial precursor CTGGCAAAACTTTCAGATGGAGTAGCTG (SEQ (Hsp60) (60 kDa chaperonin) (CPN60) (Heat ID NO: 79) shock protein 60) (HSP-60) (Mitochondrial matrix protein P1) (P60 lymphocyte protein) (HuCHA60) (LOC643288), mRNA 2 A_24_P354451 AC104825 Homo sapiens BAC clone RP11-774O3 from 4, CATAACCTTATTAATTTGCACATAGATCATCTG complete sequence. AATGTCGTGGTTTAAGACTTAAGGAGG (SEQ ID NO: 80) 2 A_24_P366465 GGATAAGATTGTCATTCAGAAATACCATCCTAA TGGCTACAACTTTGAAGTAAGAAAAGC (SEQ ID NO: 81) 2 A_24_P382113 NM_006107 CROP Homo sapiens cisplatin resistance-associated GCAGAGTGAAGACACAAACACTGAATCGAAGG overexpressed protein (CROP), transcript variant AAAGTGATACTAAGAATGAGGTCAATGG (SEQ 2, mRNA ID NO: 82) 2 A_24_P385341 NM_014388 C1orf107 Homo sapiens chromosome 1 open reading frame TTTCTATGAACTGCCGACATATCCACACTTTTA 107 (C1orf107), mRNA CAGTGAAATCTGTAATATGCTGAGAGC (SEQ ID NO: 83) 2 A_24_P388528 NM_003032 ST6GAL1 Homo sapiens ST6 beta-galactosamide alpha-2,6- ATGCAAATTATGATATGGACGTTATCATTGGTC sialytransferase 1 (ST6GAL1), TGGTGAGATGTTTCATATTTGTGACAG (SEQ ID transcript variant 2, mRNA NO: 84) 2 A_24_P393838 NM_014765 TOMM20 Homo sapiens translocase of outer mitochondrial CTAGCTGTGTCGAGTTAAGAAAAAATCAGCA membrane 20 homolog (yeast) (TOMM20), mRNA GTTTTTTCTCCCAGAAATGTAATTGCCA (SEQ ID NO: 85) 2 A_24_P402690 NM_001012514 ITM2C Homo sapiens integral membrane protein 2C ACTCTTAAATGCTTTGTATATTTTCTCAATTAGA (ITM2C), transcript variant 3, mRNA TCTCTTTTCAGAAGTGTCTATAGAAC (SEQ ID NO: 86) 2 A_24_P419300 AC010442 Homo sapiens chromosome 5 clone CTD-2228K2, TTACAGAGTTCAATATACTGTGTACCATTGATC complete sequence. TTCTATTGTGAAAGCAAAGAATTTCAT (SEQ ID NO: 87) 2 A_24_P472455 HSM801157 Homo sapiens mRNA; cDNA DKFZp564M0264 ACCCTCATGTTAAATCTTAAATGTAGTATTTCT (from clone DKFZp564M0264). AACTTGTGAAGACAGATTGGTAGGCAG (SEQ ID NO: 88) 2 A_24_P4877 NM_033114 ZCRB1 Homo sapiens zinc finger CCHC-type and RNA GAAAAATTAATACTATCATGTTAATACTATTATT binding motif 1 (ZCRB1), mRNA GTCATCCCAAGAAAAAAGATATTTTA (SEQ ID NO: 89) 2 A_24_P542375 NM_002823 PTMA Homo sapiens prothymosin, alpha (gene sequence ACTATAAGTAGTTGGTTTGTATGAGATGGTTAA 28) (PTMA), mRNA AAAGGCCAAAGATAAAAGGTTTCTTTT (SEQ ID NO: 90) 2 A_24_P579826 AC090419 Homo sapiens chromosome 17, clone CTD- GAAGAAAAGTATAAGAGTTGCTAGGTGTGACA 2107B16, complete sequence. ATCTCAAGACTTTTCAACCACTACAAAT (SEQ ID NO: 91) 2 A_24_P59239 CATCATCAACACCAAAAAAGGACAAGAATCCTT CAAAACAGGAAAAAACTCCTAAAACAC (SEQ ID NO: 92) 2 A_24_P595460 AK097398 Homo sapiens cDNA FLJ40079 fis, clone AAATTGTATGTGATATTCCAACAGCAAGTTGGA TESTI2001498, highly similar to DNA-BINDING TGCAATGTGTCATAAAAATGACCTCAG (SEQ ID PROTEIN NEFA PRECURSOR. NO: 93) 2 A_24_P6725 NM_001010914 LOC400986 Homo sapiens protein immuno-reactive with anti- AATCTGGGACAGTGTCTCCTCAGAAACAATCA PTH polyclonal antibodies (LOC400986), mRNA GCCTGGAAGGTTATATTTAAAAAGAAAG (SEQ ID NO: 94) 2 A_24_P686992 NM_001010914 LOC400986 Homo sapiens protein immuno-reactive with anti- TCCAGGAAAAGTGTCTTCTCAGAAACAACCAG PTH polyclonal antibodies (LOC400986), mRNA CTGAGAAGGCTACAAGTGACGACAAAGA (SEQ ID NO: 95) 2 A_24_P736638 NM_002156 HSPD1 K (LOC646447), mRNA GTTGAGAAAATTATGCAAAGTTCCTCAGAAGTT GGTTATGATACTATGTTAGGAGATGTC (SEQ ID NO: 96) 2 A_24_P808100 AC011890 Homo sapiens PAC clone RP4-655L22 from Xq23, TAAAAGTCAGGTTGCAGTTTCCATTGCATTCAA complete sequence. GAAAATCAGAAAAATAAATACAACTTT (SEQ ID NO: 97) 2 A_24_P82142 NM_003205 TCF12 Homo sapiens transcription factor 12 TCAGGATGATTCCTAACAAGTCAGTCATTTGTG (HTF4, helix-loop-helix transcription factors 4) AACTTAGTGGACTTTTTGGTTACTTTA (SEQ ID (TCF12), transcript variant 3, mRNA NO: 98) 2 A_24_P832113 NM_001004419 CLEC2D Homo sapiens C-type lectin domain family 2, CTTTGAAATAACACCACCAGTAGTCTTACGGTT member D (CLEC2D), transcript variant 2, mRNA GAAGTGTGGTTCAGGGCCAGTGCATAT (SEQ ID NO: 99) 2 A_24_P883109 AC073089 Homo sapiens BAC clone RP11-324F21 from 7, GGGCAACTAGTCATCTACTAGTTAGCTTAGTA complete sequence. AGCTAAGCATTAAATCTAAGAAATAGCA (SEQ ID NO: 100) 2 A_24_P927189 NM_138381 OXNAD1 oxidoreductase NAD-binding domain containing 1 AGTGTGTTGTCGTTATTAATTTGCTATTCCTTG TCCTATTCAGAAAGGATTTCAAGAGGC (SEQ ID NO: 101) 2 A_24_P930963 AC009041 Homo sapiens chromosome 16 clone RP11- GCCCCATTTCAAGTATAACCAGGAGGGAAAAT 161M6, complete sequence. GGTGCTTGAAATAAGCATGCCACAAAGG (SEQ ID NO: 102) 2 A_24_P941188 XM_375697 OTUD3 PREDICTED: Homo sapiens OTU domain CCACGGATTGTGTTCATCTGAACCATTTTATTT containing 3 (OTUD3), mRNA TTTATTTACCAAAGTACTGTACTTGGC (SEQ ID NO: 103) 2 A_24_P943263 NM_006989 RASA4 Homo sapiens RAS p21 protein activator 4 TCCTGCATAGTCTATCTTTGTATATCTTTGAAC (RASA4), mRNA TTTTCAAGAATAAAAAAGCTTAAAAAG (SEQ ID NO: 104) 2 A_32_P119604 AC090948 Homo sapiens chromosome 3 clone RP11-415F23 CAGAACTCTACTTCAGCAGACACTCAACTCAA map 3p, complete sequence. AAAGACTGGCAAATGGACATGTATTTAC (SEQ ID NO: 105) 2 A_32_P133213 AC006480 Homo sapiens BAC clone RP11-166O4 from 7, TCAAGAGAGATCCTAAAGAAAGCAAAATCACT complete sequence. GTGGACTGAAATGAGCAGACAAGGTTTT (SEQ ID NO: 106) 2 A_32_P149492 XM_496391 NBPF9 PREDICTED: Homo sapiens neuroblastoma TTCTGGATTGTTTTTTACATTCAGTGTTATAATA breakpoint family, member 9, transcript variant 1 TTTGATTATGCTGATTGGTTTTGGTG (SEQ ID (NBPF9), mRNA NO: 107) 2 A_32_P155506 NM_152653 UBE2E2 Homo sapiens ubiquitin-conjugating enzyme E2E 2 TGCAAACAATGTTGGAGCTGTAATAGTAAGAG (UBC4/5 homolog, yeast) (UBE2E2), mRNA CTTTCTTACAAAGCTTTGTATTACTGTG (SEQ ID NO: 108) 2 A_32_P159787 NM_005520 HNRPH1 Homo sapiens heterogeneous nuclear AAATAAAAGCATGTCTTTCAACATGCATCCAAA ribonucleoprotein H1 (H) (HNRPH1), mRNA ACAGTGTTCAATTTAACGTGGCAAAGG (SEQ ID NO: 109) 2 A_32_P162306 NM_001004419 CLEC2D Homo sapiens C-type lectin domain family 2, GCTGACAAAGATGATCACTTTAAGGTGGATAA member D (CLEC2D), transcript variant 2, mRNA TGATGAAAATGAGCACCAGTTATCTTTA (SEQ ID NO: 110) 2 A_32_P181548 AC087407 Homo sapiens 3 BAC CTC-269B10 (CalTech ATATTCTTCCAATATGTAGGGGAAAAGACATAT Clone Library C) complete sequence. GAATAAGACAAATGAAAAATTGCATAT (SEQ ID NO: 111) 2 A_32_P187009 AC010260 Homo sapiens chromosome 5 clone CTC-458l2, ATTCACATGAGTAAAATGATGGAAGAACTCTTT complete sequence. AAGGTAATCCTTTGGGATAAAGGATCC (SEQ ID NO: 112) 2 A_32_P193646 NM_002139 RBMX Homo sapiens RNA binding motif protein, X-linked GACTTGTACTGGTGTTGTAACTTTCCAAGTAAA (RBMX), mRNA AGTATCCCTAAAGGCCACTTCCTATCT (SEQ ID NO: 113) 2 A_32_P217510 NM_032168 WDR75 Homo sapiens WD repeat domain 75 (WDR75), TTACCGAAAAAGTCCAGGATACAAGTAACACA mRNA GGTTTAGGAGAAGACATTATACATCAGT (SEQ ID NO: 114) 2 A_32_P225604 NM_000969 RPL5 Homo sapiens ribosomal protein L5 (RPL5), AAGCACTTCATGGGCCAGAATGTTGCAGATTA mRNA CATGCGCTACTTAATGGAAGAAGATGAC (SEQ ID NO: 115) 2 A_32_P34149 NM_005520 HNRPH1 Homo sapiens heterogeneous nuclear TGAAGACTTAAGGCCCAGTATTTTTTAATAGAA ribonucleoprotein H1 (H) (HNRPH1), mRNA TACTCATCTAGGATGTAACAGTGAAGC (SEQ ID NO: 116) 2 A_32_P49423 NM_002520 NPM1 Homo sapiens nucleophosmin (nucleolar AAACAGGAAAAAACTCCTAAAACACCTAAAAG phosphoprotein B23, numatrin) (NPM1), transcript GACCTAGTTCTGTAGAAGACATTAAAGC (SEQ variant 1, mRNA ID NO: 117) 2 A_32_P63013 HUMYY74A12 Homo sapiens full length insert cDNA clone CCCGGGAGTGTTGCAAGTTAAACTGATGAAAA YY74A12. GACGTTTAGTATTTAATTGCTCCTCATG (SEQ ID NO: 118) 2 A_32_P80068 NM_001004419 CLEC2D Homo sapiens C-type lectin domain family 2, TGAACTGCACATTGTTGAAGCAGAGGCCATGA member D (CLEC2D), transcript variant 2, mRNA ATTACGAAGGCAGTCCAATTAAAGTAAC (SEQ ID NO: 119) 3 Granulocytes 3 A_23_P11926 XR_001410 FLJ21272 PREDICTED: Homo sapiens hypothetical protein ATCTTCCTAATCTCGTGGGATCACAATATGAAT FLJ21272 (FLJ21272), misc RNA AACAAGGATGAACATAAGACACATCTG (SEQ ID NO: 120) 3 A_23_P135769 NM_001101 ACTB Homo sapiens actin, beta (ACTB), mRNA TTTAAAAACTGGAACGGTGAAGGTGACAGCAG TCGGTTGGAGCGAGCATCCCCCAAAGTT (SEQ ID NO: 121) 3 A_23_P19590 NM_003379 VIL2 Homo sapiens villin 2 (ezrin) (VIL2), mRNA GATTATTCTCGAATCACCTCCTGTGTTGTGCT GGGAGCAGGACTGATTGAATTACGGAAA (SEQ ID NO: 122) 3 A_23_P20894 NM_024757 EHMT1 Homo sapiens euchromatic histone-lysine N- TGATTTCAGACTCAGAAGCCGACGTTCGAGAG methyltransferase 1 (EHMT1), mRNA GAAGATTCTTACCTCTTTGATCTCGACA (SEQ ID NO: 123) 3 A_23_P257503 NM_003922 HERC1 Homo sapiens hect (homologous to the E6-AP TTTGGTCACTTTTGATAAGTTTGCATGAAACCA (UBE3A) carboxyl terminus) domain and RCC1 TTTTGGTGCATTTTTAGTTGGGAATGG (SEQ ID (CHC1)-like domain (RLD) 1 (HERC1), mRNA NO: 124) 3 A_23_P259901 NM_012253 TKTL1 Homo sapiens transketolase-like 1 (TKTL1), GATGTCCTGTGCTGCTTGTGATGAGAGCCTCC mRNA ACACTGTACTGTTCAAGTCAATGTTAAT (SEQ ID NO: 125) 3 A_23_P26759 NM_138793 CANT1 Homo sapiens calcium activated nucleotidase 1 AATGTTGCCTTTTTCTAGGAACTGTCAGAAATC (CANT1), mRNA CTCATGCCTTTCAAGACTTCTGTGAAT (SEQ ID NO: 126) 3 A_23_P31686 NM_021174 KIAA1967 Homo sapiens KIAA1967 (KIAA1967), transcript AGAAAAAGGCTTTTCGAGTGTGGGACAAGGTC variant 1, mRNA TGATGTCAGTGAACGGAATTGAAGAGCA (SEQ ID NO: 127) 3 A_23_P319895 XM_037523 KIAA1076 PREDICTED: Homo sapiens KIAA1076 protein TGCAACTGAGGAAATAATTTATTTTTCACATGA (KIAA1076), mRNA GGAAATGCGTAGCTTGTAGAGACGGCT (SEQ ID NO: 128) 3 A_23_P332190 NM_002163 IRF8 Homo sapiens interferon regulatory factor 8 GGGATGCCTTACTTTGCACTTAATTTAATAAGG (IRF8), mRNA GCATTCTCGGAGGAGTAGACGTTTAAT (SEQ ID NO: 129) 3 A_23_P359430 NM_015383 NBPF14 Homo sapiens neuroblastoma breakpoint family, ACCCTGGTTTCAATGAACCTAACCTCATTCTTT member 14 (NBPF14), mRNA GTGTCTTCAGTGTTGGCTTGTTTTAGC (SEQ ID NO: 130) 3 A_23_P388681 NM_001419 ELAVL1 Homo sapiens ELAV (embryonic lethal, abnormal AGATAATTAAGAGTGAAGGAGTTGAAACTTTTC vision, Drosophila)-like 1 (Hu antigen R) TTGTTAGTGTACAACTCATTTTGCGCC (SEQ ID (ELAVL1), mRNA NO: 131) 3 A_23_P406330 NM_022733 SMAP1L Homo sapiens stromal membrane-associated CAGCAGCCTAAAACTGTTGTGTTTTTCTTATGG protein 1-like (SMAP1L), mRNA TTTAAAAAACGCCATGTCATTGATAAC (SEQ ID NO: 132) 3 A_23_P416434 NM_015288 PHF15 Homo sapiens PHD finger protein 15(PHF15), ATATATTGAAAAGAGCAATTTTAAATTATTTTTG mRNA GCTTATGTTGCAATATTTATTTTCTT (SEQ ID NO: 133) 3 A_23_P417200 NM_005652 TERF2 Homo sapiens telomeric repeat binding factor 2 TCCCTGGTAATCTGTAGAACCTTCTCCTAGGA (TERF2), mRNA AATGGTGAAGTCTATTAGGAGCCACTTG (SEQ ID NO: 134) 3 A_23_P44581 NM_001004060 NOMO2 Homo sapiens NODAL modulator 2 (NOMO2), AATGTGATCACTTCCTCTGAATACCTTCCTACA transcript variant 1, mRNA TTATGGGTCAAGCTTTACAAAAGCGAA (SEQ ID NO: 135) 3 A_23_P44734 NM_032557 USP38 Homo sapiens ubiquitin specific peptidase 38 GGATGCTATAACAAAAGACAATAAACTATATTT (USP38), mRNA ACAGGAACAAGAGTTGAATGCTCGAGC (SEQ ID NO: 136) 3 A_23_P60354 NM_003070 SMARCA2 Homo sapiens SWI/SNF related, matrix TATCATCATCGTCTATAAACTAGCTTTAGGATA associated, actin dependent regulator of GTGCCAGACAAACATATGATATCATGG (SEQ chromatin, subfamily a, member 2 (SMARCA2), ID NO: 137) transcript variant 1, mRNA 3 A_23_P73593 NM_002444 MSN Homo sapiens moesin (MSN), mRNA GAAGCTTTCAGTATTAGTGATGTCATCTGTCAC TATAGGTCATACAATCCATTCTTAAAG (SEQ ID NO: 138) 3 A_23_P97770 NM_020216 RNPEP Homo sapiens arginyl aminopeptidase ACCAGGAAGATTTCTGGAAAGTGAAGGAGTTC (aminopeptidase B) (RNPEP), mRNA CTGCATAACCAGGGGAAGCAGAAGTATA (SEQ ID NO: 139) 3 A_24_P174257 NM_019044 CCDC93 coiled-coil domain containing 93 AAAGAGAGGGAAGAACTACACTAATGTTAGAG ATAAGGTATGTTTTGGCTCAAAATGTGT (SEQ ID NO: 140) 3 A_24_P18190 NM_005347 HSPA5 Homo sapiens heat shock 70 kDa protein 5 TTCTACAGCTTCTGATAATCAACCAACTGTTAC (glucose-regulated protein, 78 kDa) (HSPA5), AATCAAGGTCTATGAAGGTGAAAGACC (SEQ mRNA ID NO: 141) 3 A_24_P186030 NM_002760 PRKY Homo sapiens protein kinase, Y-linked (PRKY), CCAGTTTTCTCTGTACCTGTGTGTATAGAAATA mRNA GATCAGAGCACAGTTGAAATTCATGGA (SEQ ID NO: 142) 3 A_24_P187626 AC055811 Homo sapiens chromosome 17, clone RP11- GAAGTGTGATGTGGACATCTGCAAAGACTTAT 45M22, complete sequence. ATGCCAACGTGCTGTCTGGCGGCACCAC (SEQ ID NO: 143) 3 A_24_P222599 NM_002613 PDPK1 Homo sapiens 3-phosphoinositide dependent GCTGGTAAAAGCCTCTATTACGACTGTAAGTA protein kinase-1 (PDPK1), transcript variant 1, AGTTGGATGTTGGCAAAATTAAATTGTT (SEQ mRNA ID NO: 144) 3 A_24_P225325 NM_022733 SMAP1L Homo sapiens stromal membrane-associated CATGTTCTCATGATTTATGGGAATGAAGCAAGT protein 1-like (SMAP1L), mRNA ACTGAAATCAAATTAAATACTCCCTGG (SEQ ID NO: 145) 3 A_24_P226037 NM_001003810 HNRPD Homo sapiens heterogeneous nuclear AGAAATACCACAATGTTGGTCTTAGTAAATGTG ribonucleoprotein D (AU-rich element RNA binding AAATAAAAGTAGCCATGTCGAAGGAAC (SEQ protein 1, 37 kDa) (HNRPD), transcript variant 4, ID NO: 146) mRNA 3 A_24_P226554 NM_001101 ACTB Homo sapiens actin, beta (ACTB), mRNA GCACCCAGCACAATGAAGATCAAGATCATTGC TCCTCCTGAGCGCAAGTACTCCGTGTGG (SEQ ID NO: 147) 3 A_24_P238744 XM_292982 LOC653269 PREDICTED: Homo sapiens similar to protein TGTGGCATCCACGAAACTACCTTCAACTCCAT expressed in prostate, ovary, testis, and CATGAAGTCGGATGTGGACATCTACAAA (SEQ placenta 15, transcript variant 1 ID NO: 148) (LOC653269), mRNA 3 A_24_P255786 AL359844 Human DNA sequence from clone RP11-314J18 GTCCTCCTGGGAGAAGAGCTATGAGCTGTCA on chromosome 10 GATGGCCAGGTCATCACCAGCAGCAACAA (SEQ ID NO: 149) 3 A_24_P261169 NM_006378 SEMA4D Homo sapiens sema domain, immunoglobulin AACTTCCTTTTGCTAAATGCATTCTTTCTGCTTT domain (Ig), transmembrane domain (TM) and TAGAAATGTAGACATAAACACTCCCC (SEQ ID short cytoplasmic domain, (semaphorin) 4D NO: 150) (SEMA4D), mRNA 3 A_24_P273666 NM_000516 GNAS Homo sapiens GNAS complex locus (GNAS), CCCCGAGTGATTTTGCGAAACCCCCTTTTCCC transcript variant 1, mRNA TTCAGCTTGCTTAGATGTTCCAAATTTA (SEQ ID NO: 151) 3 A_24_P287272 XM_498427 NBPF1 PREDICTED: Homo sapiens neuroblastoma ACCTAACCTCATTCTTTGTATCTTCAGTGTTGA breakpoint family, member 1, transcript variant 1 ATTGTTTTAGCTGATCCATCTTTAACG (SEQ ID (NBPF1), mRNA NO: 152) 3 A_24_P325333 NM_002600 PDE4B Homo sapiens phosphodiesterase 4B, cAMP- ACTTCTACACAGATAAGCTTTCAAAGTTGACAA specific (phosphodiesterase E4 dunce homolog, ACTTTTTTGACTCTTTCTGGAAAAGGG (SEQ ID Drosophila) (PDE4B), mRNA NO: 153) 3 A_24_P331998 NM_203447 DOCK8 Homo sapiens dedicator of cytokinesis 8 (DOCK8), CCTACATACAGATCACTTTTGTGGAGCCCTAC mRNA TTTGATGAGTATGAGATGAAAGACAGGG (SEQ ID NO: 154) 3 A_24_P354724 NM_054114 TAGAP Homo sapiens T-cell activation GTPase activating GGCCATACGCCATGCCATAGCTTGTGCTATCT protein (TAGAP), transcript variant 2, mRNA GTAAATATGAGACTTGTAAAGAACTGCC (SEQ ID NO: 155) 3 A_24_P369154 NM_002721 PPP6C Homo sapiens protein phosphatase 6, catalytic AATATTGCTTCGATCATGGTCTTCAAAGATGTA subunit (PPP6C), mRNA AATACAAGAGAACCAAAGTTATTCCGG (SEQ ID NO: 156) 3 A_24_P375076 AL390237 Human DNA sequence from clone RP11-278J20 GACAATATTATGCAAGTGTGGCAAATGGCAGA on chromosome 6 Contains a retinoblastoma GAACATTTACAACAATGAAGACCCTGAA (SEQ binding protein 4 (RBBP4) pseudogene and a ID NO: 157) KIAA0797 pseudogene, complete sequence. 3 A_24_P383901 HSBA12M9 Human DNA sequence from clone RP11-12M9 on CATGTACCCTGGCATCACCAACAGGATGCAGA chromosome 22, complete sequence. AGAAGATCACCGCCCTAGCACCCAGCAT (SEQ ID NO: 158) 3 A_24_P391568 NM_001668 ARNT Homo sapiens aryl hydrocarbon receptor nuclear GGCTTTGGCCAGTAGCTAAAGTGCAAGACTGA translocator (ARNT), transcript variant 1, mRNA ATTAATGAGAAGATATATTAAATGTAGT (SEQ ID NO: 159) 3 A_24_P393151 AC009892 Homo sapiens chromosome 19 clone CTB-83J4, AAGAAATCTTATCATTCGCCATCTACCCTGTAG complete sequence. AATAAAGAAATCTTATCATTCACCGTC (SEQ ID NO: 160) 3 A_24_P401090 AL354702 Human DNA sequence from clone RP11-334L9 on TTTTCTACAGCTTTTGATAATCAAGTTACAATC chromosome 1 Contains a heat shock 70 kDa AAGGTCTATGAAGGTAAACAACCCCTG (SEQ protein 5 (glucose-regulated protein, 78 kDa) ID NO: 161) (HSPA5) pseudogene, complete sequence. 3 A_24_P408424 NM_002473 MYH9 Homo sapiens myosin, heavy polypeptide 9, non- CTGGTCTACACTGGTTGCCGAATTTACTTGTAT muscle (MYH9), mRNA TCCTAACTGTTTTGTATATGCTGCATT (SEQ ID NO: 162) 3 A_24_P410017 NM_001017421 FKSG30 Homo sapiens actin-like protein (FKSG30), mRNA ATGAAACTACCTTCAACTCCATCATGAAGTCTG ATGTGGACATCCGCAAAGACCTGTACA (SEQ ID NO: 163) 3 A_24_P42517 NM_006854 KDELR2 Homo sapiens KDEL (Lys-Asp-Glu-Leu) CATCCTATACTGTGACTTCTTCTACTTGTACAT endoplasmic reticulum protein retention TACAAAAGTACTCAAGGGAAAGAAGCT (SEQ receptor 2 (KDELR2), mRNA ID NO: 164) 3 A_24_P47182 NM_003373 VCL Homo sapiens vinculin (VCL), transcript ATGGGGTTCAAGAGAGTAATGGGTTTCATATT variant 2, mRNA TCTTATCACCACAGTAAGTTCCTACTAG (SEQ ID NO: 165) 3 A_24_P475115 AC097103 Homo sapiens 3 BAC RP11-319G6 (Roswell Park ACTGACTACTTCATGAAGATCCTCATGGAGTG Cancer Institute Human BAC Library) complete CAGCTACCGTTTCACCACCATGGCTGAG (SEQ sequence ID NO: 166) 3 A_24_P63118 NM_013374 PDCD6IP Homo sapiens programmed cell death 6 TAGTTTTTGCACGGAAGACAGAAAGAGATGAA interacting protein (PDCD6IP), mRNA CTCTTAAAGGACTTGCAACAAAGCATTG (SEQ ID NO: 167) 3 3 Granulocyte A_24_P63136 NM_023914 P2RY13 Homo sapiens purinergic receptor P2Y, G-protein ATGCCAGATTTTCTTGGTATCTCCCATAATACG coupled, 13 (P2RY13), transcript variant 1, mRNA ACCTACAGTCCATGGTCTACAGATGTT (SEQ ID NO: 168) 3 A_24_P63827 NM_005494 DNAJB6 Homo sapiens DnaJ (Hsp40) homolog, subfamily CAACTTCAACTAAAATGGTTAATGGCAGAAAAA B, member 6 (DNAJB6), transcript variant 2, TCACTACAAAGAGAATTGTCGAGAACG (SEQ mRNA ID NO: 169) 3 A_24_P643587 NM_024095 ASB8 Homo sapiens ankyrin repeat and SOCS box- GCTCTGTAATAACAGTAATAAATAGCTCTGAAA containing 8 (ASB8), mRNA TAACAGTCCTAAGAACTCCTAAAGTCC (SEQ ID NO: 170) 3 A_24_P681011 HSM807522 Homo sapiens mRNA; cDNA DKFZp686K02111 GTGTTAATCCATGTTAATCTGTGTGAAAATTAT (from clone DKFZp686K02111). TGCGTGCAACAGTATTTTCTCGTGTAC (SEQ ID NO: 171) 3 A_24_P68649 NM_020216 RNPEP Homo sapiens arginyl aminopeptidase GCAACAGGAGAGAAGCTTTTTGGACCTTATGT (aminopeptidase B) (RNPEP), mRNA TTGGGGAAGGTATGACTTGCTCTTCATG (SEQ ID NO: 172) 3 A_24_P693321 ATCACAACTATGCCAAATAATCAATCCTACAAT GTCCAAAATTTTACTTTAAAACTGGAA (SEQ ID NO: 173) 3 A_24_P714134 XR_019310 LOC646447 PREDICTED: Homo sapiens similar to AGAGTGCATAAAATTATCCTTGATCTTATATCT heterogeneous nuclear ribonucleoprotein GAGTCTCCTACAGAGGATGTGCACAGA (SEQ ID NO: 174) 3 A_24_P787897 XM_001125986 LOC283824 PREDICTED: Homo sapiens hypothetical protein TGAACTATCTGAAATTGACCAGTAATCAAAGTT LOC283824 CCAATCATCTGAATGCTTTTCCTTGAG (SEQ ID NO: 175) 3 A_24_P79617 NM_014656 KIAA0040 Homo sapiens KIAA0040 (KIAA0040), mRNA TGAAAATGAAAAGTCTTGATGTAGTCAGATGG TTACTCTCTTAACATTAGGTATTACCCC (SEQ ID NO: 176) 3 A_24_P7974 AF161369 Homo sapiens HSPC106 mRNA, partial cds. GTTGCTTTATGTAGCAAATTCTCCGTTTGGAG CTTTTAAAATAGGATTATTTGCCAGAAC (SEQ ID NO: 177) 3 A_24_P808534 NM_001357 DHX9 Homo sapiens DEAH (Asp-Glu-Ala-His) box GGAAAAGACAAAGATTCTCACCACTGAAGGGT polypeptide 9 (DHX9), transcript variant 1, mRNA GTAATGCACTTATCCACAAATCATCTGT (SEQ ID NO: 178) 3 A_24_P940059 NM_015553 PIP3-E Homo sapiens phosphoinositide-binding protein CCCAGGGTTTTGTAATACATAATTGAAAATAAA PIP3-E (PIP3-E), mRNA AGTCCCTGAAACTAAATGTTTGCAGCC (SEQ ID NO: 179) 3 A_32_P11359 AACTAAAAAGCATTAATTAAAAAGTACTTAACT CAGAAATTATAAAAATAGGAGACATCA (SEQ ID NO: 180) 3 A_32_P144920 NM_015509 NECAP1 Homo sapiens NECAP endocytosis associated 1 TTGAGTTTGAATTGTGTAACATCTTTGATCAGT (NECAP1), mRNA GGGTGTATCTGTAATGAAGGAGGTTCA (SEQ ID NO: 181) 3 A_32_P155776 NM_001017421 FKSG30 Homo sapiens actin-like protein (FKSG30), mRNA ATAGTGAAGTCTGATGTGGACATCCGCAAAGA CCTGTACACCAACACAGTGCTGTCTGGC (SEQ ID NO: 182) 3 A_32_P221958 NM_133446 CTGLF1 Homo sapiens centaurin, gamma-like family, ATGGGAAAAATAAGGATAACTCAGAATTTCAAA member 1 (CTGLF1), mRNA AGGAAATCACAAATTCAGCTAGTAATA (SEQ ID NO: 183) 3 A_32_P60551 HS661I20 Human DNA sequence from clone RP4-661I20 on GCAGAAGTACAAGCTTTAGGGTGTATCTATTC chromosome 20q11.23-12 Contains the RPL12L2 ATCTATTCCTAGTACATAAAATTTAGCC (SEQ gene for ribosomal protein L12-like 2 pseudogene, ID NO: 184) the 5′ end of the CHD6 gene for chromodomain helicase DNA binding protein 6 and two CpG islands, complete sequence. 3 A_32_P79434 NM_002847 PTPRN2 Homo sapiens protein tyrosine phosphatase, TCTCTACATGGTATTGTAATGAATATCTGCTTT receptor type, N polypeptide 2 (PTPRN2), AATATAGCTATCATTTCTTTTCCAAAA (SEQ ID transcript variant 1, mRNA NO: 185) 3 A_32_P8666 NM_002140 HNRPK Homo sapiens heterogeneous nuclear GGTCTGCAGATTAAACAAATCCGTCATGAGTC ribonucleoprotein K (HNRPK), transcript GGGAGCTTCGATCAAAATTGATGAGCCT (SEQ variant 1, mRNA ID NO: 186) 4 Granulocytes 4 A_23_P113762 AGACGCTGGACGAAGATGGGGATGGGGAGTG TGACTTCCAGGAGTTTATGGCCTTCGTCT (SEQ ID NO: 187) 4 A_23_P117992 NM_014861 KIAA0703 Homo sapiens KIAA0703 gene product TCCATCACCGGATCAGTTTTTCCTCTTAGGAAA (KIAA0703), mRNA GCTGCAGGAACCTCGTGGGCTCCAGGG (SEQ ID NO: 188) 4 A_23_P119222 NM_020415 RETN Homo sapiens resistin (RETN), mRNA CAATAAGCAGCATTGGCCTGGAGTGCCAGAG CGTCACCTCCAGGGGGGACCTGGCTACTT (SEQ ID NO: 189) 4 2 Granulocyte A_23_P121622 NM_014465 SULT1B1 Homo sapiens sulfotransferase family, cytosolic, GAAATAGAGATTGTCTGTAGTTGATTGAAACG 1B, member 1 (SULT1B1), mRNA AGGGCAGTTATGAATTGATTTGGGCAAT (SEQ ID NO: 190) 4 8 Granulocyte A_23_P121716 NM_005139 ANXA3 Homo sapiens annexin A3 (ANXA3), mRNA TGGACATTCGAACAGAGTTCAAGAAGCATTAT GGCTATTCCCTATATTCAGCAATTAAAT (SEQ ID NO: 191) 4 A_23_P122924 NM_002192 INHBA Homo sapiens inhibin, beta A (activin A, AAACATCATCAAAAAGGACATTCAGAACATGAT activin AB alpha polypeptide) (INHBA), mRNA CGTGGAGGAGTGTGGGTGCTCATAGAG (SEQ ID NO: 192) 4 A_23_P123645 AATGGTTTTGTGCAGTGAACAACACATGGCGA GGTACTAACTGAGAAACTTTTTCATGCT (SEQ ID NO: 193) 4 A_23_P126278 NM_003465 CHIT1 Homo sapiens chitinase 1 (chitotriosidase) GGGCCACCAAACAGAGAATCCAGGATCAGAA (CHIT1), mRNA GGTGCCCTACATCTTCCGGGACAACCAGT (SEQ ID NO: 194) 4 A_23_P130961 NM_001972 ELA2 Homo sapiens elastase 2, neutrophil (ELA2), AACGGCTACGACCCCGTAAACTTGCTCAACGA mRNA CATCGTGATTCTCCAGCTCAACGGGTCG (SEQ ID NO: 195) 4 4 Granulocyte A_23_P131785 NM_001725 BPI Homo sapiens bactericidal/permeability-increasing GACTCAGATTCAGAAATGATCTAAACACGAGG protein (BPI), mRNA AAACATTATTCATTGGAAAAGTGCATGG (SEQ ID NO: 196) 4 A_23_P140384 NM_001911 CTSG Homo sapiens cathepsin C (CTSG), mRNA TGTGACTGACTCTTCTTCTCGGGGACACAGGC CAGCTCCACAGTGTTGCCAGAGCCTTAA (SEQ ID NO: 197) 4 A_23_P141173 NM_000250 MPO Homo sapiens myeloperoxidase (MPO), nuclear CCTGTTCTGGGTGCAGCTGAGAAAATGAGTGA gene encoding mitochondrial protein, mRNA CTAGACGTTCATTTGTGTGCTCATGTAT (SEQ ID NO: 198) 4 A_23_P149301 NM_002105 H2AFX Homo sapiens H2A histone family, member X GGCGCGCGACAACAAGAAGACGCGCATCATC (H2AFX), mRNA CCGCGCCACCTGCACCTGGCCATCCGCAA (SEQ ID NO: 199) 4 A_23_P151637 NM_002934 RNASE2 Homo sapiens ribonuclease, RNase A family, 2 GTGGTAACCCAAATATGACCTGTCCTAGTAAC (liver, eosinophil-derived neurotoxin) (RNASE2), AAAACTCGCAAAAATTGTCACCACAGTG (SEQ mRNA ID NO: 200) 4 3 Granulocyte A_23_P156180 NM_003059 SLC22A4 Homo sapiens solute carrier family 22 (organic AAACAAGAGACTCAATGGAGACAGAAGAAAAT cation transporter), member 4 (SLC22A4), mRNA CCCAAGGTTCTAATAACTGCATTCTGAA (SEQ ID NO: 201) 4 A_23_P161428 NM_144590 ANKRD22 Homo sapiens ankyrin repeat domain 22 AATCCTTGTGACCACACCGATGGAGATACAGA (ANKRD22), mRNA AAAAGTTAACGACTGGATTCTATCTTCA (SEQ ID NO: 202) 4 A_23_P163025 NM_002934 RNASE2 Homo sapiens ribonuclease, RNase A family, 2 AGCCACAGCTCAGAGACTGGGAAACATGGTTC (liver, eosinophil-derived neurotoxin) (RNASE2), CAAAACTGTTCACTTCCCAAATTTGTCT (SEQ mRNA ID NO: 203) 4 4 Granulocyte A_23_P166848 NM_002343 LTF Homo sapiens lactotransferrin (LTF), mRNA ATATTTGGGACCACAGTATGTCGCAGGCATTA CTAATCTGAAAAAGTGCTCAACCTCCCC (SEQ ID NO: 204) 4 A_23_P168014 NM_003509 HIST1H2AI Homo sapiens histone 1, H2ai (HIST1H2AI), TGAGGAGCTCAACAAGCTTCTGGGCAAACTCA mRNA CCATCGCACAGGGTGGCGTCCTGCCCAA (SEQ ID NO: 205) 4 A_23_P169437 NM_005564 LCN2 Homo sapiens lipocalin 2 (oncogene 24p3) GCTATGGTGTTCTTCAAGAAAGTTTCTCAAAAC (LCN2), mRNA AGGGAGTACTTCAAGATCACCCTCTAC (SEQ ID NO: 206) 4 A_23_P170233 NM_005213 CSTA Homo sapiens cystatin A (sterin A) (CSTA), mRNA AACTGGCTACTGAGTCATGATCCTTGCTGATA AATATAACCATCAATAAAGAAGCATTCT (SEQ ID NO: 207) 4 A_23_P19543 NM_003137 SRPK1 Homo sapiens SFRS protein kinase 1 (SRPK1), CTGTCAAATTGCCACGATCTCACTAAAGGATTT mRNA CTATTTGCTGTCAGTTAAAATAAAGC (SEQ ID NO: 208) 4 A_23_P200507 NM_014184 CNIH4 Homo sapiens cornichon homolog 4 (Drosophila) TGGTTGAAGTCAGCCTACACTACAGTGCACAG (CNIH4), mRNA TTGAGGAGCCAGAGACTTAAATCAT (SEQ ID NO: 209) 4 A_23_P206760 NM_005143 HP Homo sapiens haptoglobin (HP), mRNA GATAAGATGTGGTTTGAAGCTGATGGGTGCCA GCCCTGCATTGCTGAGTCAATCAATAAA (SEQ ID NO: 210) 4 3 Granulocyte A_23_P218442 NM_002483 CEACAM6 Homo sapiens carcinoembryonic antigen-related ACACTCATCTGACTCATTCTTTATTCTATTTTAG cell adhesion molecule 6 (non-specific cross TTGGTTTGTATCTTGCCTAAGGTGCG (SEQ ID reacting antigen) (CEACAM6), mRNA NO: 211) 4 A_23_P23048 NM_002965 S100A9 Homo sapiens S100 calcium binding protein A9 GAGCTGGTGCGAAAAGATCTGCAAAATTTTCT (calgranulin B) (S100A9), mRNA CAAGAAGGAGAATAAGAATGAAAAGGTC (SEQ ID NO: 212) 4 A_23_P25235 NM_080387 CLEC4D Homo sapiens C-type lectin domain family 4, CATTTAACCCACGCAGAGTATTCTGGCATAAG member D (CLEC4D), mRNA AATGAACCCGACAACTCTCAGGGAGAAA (SEQ ID NO: 213) 4 18 Granulocyte A_23_P253791 NM_004345 CAMP Homo sapiens cathelicidin antimicrobial peptide GAATTGTCCAGAGAATCAAGGATTTTTTGCGG (CAMP), mRNA AATCTTGTACCCAGGACAGAGTCCTAGT (SEQ ID NO: 214) 4 A_23_P258493 NM_005573 LMNB1 Homo sapiens lamin B1 (LMNB1), mRNA AATATTAACCTAATCACCATGTAAGCACTCTGG ATGATGGATTCCACAAAACTTGGTTTT (SEQ ID NO: 215) 4 3 Granulocyte A_23_P259506 NM_032412 ORF1-FL49 Homo sapiens putative nuclear protein ORF1- TGGGATTCTAGATTAATGGGGGTTGCTACTGT FL49 (ORF1-FL49), mRNA TTAATTCAGTGACTTGATCTTTTTAATG (SEQ ID NO: 216) 4 A_23_P302470 NM_014465 SULT1B1 Homo sapiens sulfotransferase family, cytosolic, TGTCTAAGTCACAAATCTGAAGAAATAAGAGAT 1B, member 1 (SULT1B1), mRNA TGTCTGTAGTTGATTGAAACGAGGGCA (SEQ ID NO: 217) 4 A_23_P306941 NM_153615 Rgr Homo sapiens Ral-GDS related protein Rgr (Rgr), CCATGGGACTTTTGTGAGTCAGGCGGGAGAC mRNA CATTTTATGTTTATTTTCTTTAGTGTATA (SEQ ID NO: 218) 4 2 Granulocyte A_23_P309381 NM_003516 HIST2H2AA Homo sapiens histone 2, H2aa (HIST2H2AA), CGACTTTCCCGATCGCCAGGCAGGAGTTTCTC mRNA TCGGTGACTACTATCGCTGTCATGTCTG (SEQ ID NO: 219) 4 A_23_P312932 NM_175857 KRTAP8-1 Homo sapiens keratin associated protein 8-1 GGCTATGGCTTCGGCTATGGCTACAACGGCT (KRTAP8-1), mRNA GTGGGGCTTTCGGCTACAGGAGATACTCG (SEQ ID NO: 220) 4 24 Granulocyte A_23_P31816 NM_004084 DEFA1 Homo sapiens defensin, alpha 1 (DEFA1), mRNA GAGAACGTCGCTATGGAACCTGCATCTACCAG GGAAGACTCTGGGCATTCTGCTGCTGAG (SEQ ID NO: 221) 4 13 Granulocyte A_23_P326080 NM_001925 DEFA4 Homo sapiens defensin, alpha 4, corticostatin AGAGCTACAGGAAATGGTTGTTTCTCCTATACT (DEFA4), mRNA TTGTCCTTAACATCTTTCTTGATCCTA (SEQ ID NO: 222) 4 A_23_P330561 NM_174918 MCEMP1 Homo sapiens mast cell-expressed membrane CTGTCTCCCTGTTTGTGTAAACATACTAGAGTA protein 1 (MCEMP1), mRNA TACTGCGGCGTGTTTTCTGTCTACCCA (SEQ ID NO: 223) 4 A_23_P332042 NM_004259 RECQL5 Homo sapiens RecQ protein-like 5 (RECQL5), CTTTCTGCTTGCAAAGCCTATAGACCCTTCTCA transcript variant 1, mRNA GAGCGGTCCTCATGGCTGGGTTTTCTG (SEQ ID NO: 224) 4 A_23_P344973 NM_021019 MYL6 Homo sapiens myosin, light polypeptide 6, alkali, CCTATGAGGATTATGTCGAAGGACTTCGGGTG smooth muscle and non-muscle (MYL6), transcript TTTGACAAGGAAGGAAATGGCACCGTCA (SEQ variant 1, mRNA ID NO: 225) 4 2 Granulocyte A_23_P370635 NM_138799 OACT2 Homo sapiens O-acyltransferase (membrane TTGTTCCTAAATGGTATTTTCAAGTGTAATATT bound) domain containing 2 (OACT2), mRNA GTGAGAACGCTACTGCAGTAGTTGATG (SEQ ID NO: 226) 4 A_23_P371495 XM_928461 LOC653626 PREDICTED: Homo sapiens similar to ARG99 ACCAGACTAAGTGCCAGTATATATATGACTGAT protein (LOC653626), mRNA ATTTTCGTGACTCATAGAAGGTGTCCA (SEQ ID ID NO: 227) 4 5 Granulocyte A_23_P380240 NM_001816 CEACAM8 Homo sapiens carcinoembryonic antigen-related TAGTCCACCCAATGGCTGACAGTAACAGCATC cell adhesion molecule 8 (CEACAM8), mRNA TTTAACACAACTCTTTGTTCAAATGTAC (SEQ ID NO: 228) 4 A_23_P395438 NM_053044 HTRA3 Homo sapiens HtrA serine peptidase 3 (HTRA3), AAGGGGCATTTGTGAGCTTTGCTGTAAATGGA mRNA TTCCCAGTGTTGCTTGTACTGTATGTTT (SEQ ID NO: 229) 4 A_23_P4096 NM_000717 CA4 Homo sapiens carbonic anhydrase IV (CA4), TAATATCCCCAAACCTGAGATGAGCACTACGA mRNA TGGCAGAGAGCAGCCTGTTGGACCTGCT (SEQ ID NO: 230) 4 A_23_P41114 NM_005213 CSTA Homo sapiens cystatin A (stefin A) (CSTA), mRNA AAACAAATGAGACTTATGGAAAATTGGAAGCT GTGCAGTATAAAACTCAAGTTGTTGCTG (SEQ ID NO: 231) 4 A_23_P421493 NM_020995 HPR Homo sapiens haptoglobin-related protein (HPR), GGGGACAAAGTGACAACTTTAAACTTACTGAC mRNA CATCTGAAGTATGTCATGCTGCCTGTGG (SEQ ID NO: 232) 4 A_23_P434809 NM_002964 S100A8 Homo sapiens S100 calcium binding protein A8 AAAGCCATGAAGAAAGCCACAAAGAGTAGCTG (calgranulin A) (S100A8), mRNA AGTTACTGGGCCCAGAGGCTGGGCCCCT (SEQ ID NO: 233) 4 A_23_P60248 NM_003329 TXN Homo sapiens thioredoxin (TXN), mRNA GGACAAAAGGTGGGTGAATTTTCTGGAGCCAA TAAGGAAAAGCTTGAAGCCACCATTAAT (SEQ ID NO: 234) 4 A_23_P63390 NM_000566 FCGR1A Homo sapiens Fc fragment of IgG, high TTTAGTGAACACTGTTCTCTGGGTGACAATAC affinity Ia, receptor (CD64) (FCGR1A), mRNA GTAAAGAACTGAAAAGAAAGAAAAAGTG (SEQ ID NO: 235) 4 4 Granulocyte A_23_P67847 NM_024572 GALNT14 Homo sapiens UDP-N-acetyl-alpha-D- AAGCCTTCTTTTTCACTAGGCCAGGACTACATT galactosamine:polypeptide N- GAGAGATGAAGAATGGAGGTTGTTTCC (SEQ acetylgalactosaminyltransferase 14 (GalNAc-T14) ID NO: 236) (GALNT14), mRNA 4 A_23_P74001 NM_005621 S100A12 Homo sapiens S100 calcium binding protein A12 TGAAGGCTTTTTACCCAGCAATGTCCTCAATG (calgranulin C) (S100A12), mRNA AGGGTCTTTTCTTTCCCTCACCAAAACC (SEQ ID NO: 237) 4 3 B cells A_23_P85250 NM_013230 CD24 Homo sapiens CD24 antigen (small cell lung CTGCCTCGACACACATAAACCTTTTTAAAAATA carcinoma cluster 4 antigen) (CD24), mRNA GACACTCCCCGAAGTCTTTTGTTTGTA (SEQ ID NO: 238) 4 A_23_P85903 NM_003268 TLR5 Homo sapiens toll-like receptor 5 (TLR5), mRNA AACAGTAGAAAGATCGTTTGTCTTGTGAGCAG ACACTTCCTTAGAGATGGCTGGTGCCTT (SEQ ID NO: 239) 4 A_23_P94230 NM_015364 LY96 Homo sapiens lymphocyte antigen 96 (LY96), TGAAGCTATTTCTGGGAGCCCAGAAGAAATGC mRNA TCTTTTGCTTGGAGTTTGTCATCCTACA (SEQ ID NO: 240) 4 3 Granulocyte A_23_P99253 NM_004664 LIN7A Homo sapiens lin-7 homolog A (C. elegans) TTGAGGGAAAGCTACTTGATCAAACATCCGAT (LIN7A), mRNA AGTCACAAATTTGAAACCGTGCTTCAGA (SEQ ID NO: 241) 4 A_24_P145066 NM_183416 KIF1B Homo sapiens kinesin family member 1B (KIF1B), TAGCTAGAACAGTTGAAGTCTTCAACTGAGGT transcript variant 2, mRNA TTTATAGCAGATTAGACATGGGTAAATG (SEQ ID NO: 242) 4 33 Granulocyte A_24_P181254 NM_006418 OLFM4 Homo sapiens olfactomedin 4 (OLFM4), mRNA TTTTTCCTTTGATGTTCAAGTCCTAGTCTATAG GATTGGCAGTTTAAATGCTTTACTCCC (SEQ ID NO: 243) 4 A_24_P252996 NM_000804 FOLR3 Homo sapiens folate receptor 3 (gamma) CCTGCAAAAGCAACTGGCACAAAGGCTGGAAT (FOLR3), mRNA TGGACCTCAGGGATTAATGAGTGTCCGG (SEQ ID NO: 244) 4 A_24_P273143 NM_052871 MGC4677 Homo sapiens hypothetical protein MGC4677 ACAGGAAGCTCTATGACACACTTGATCGAATA (MGC4677), mRNA TGACAGACACCGAAAATCACGACTCAGC (SEQ ID NO: 245) 4 A_24_P52004 NM_015200 SCC-112 Homo sapiens SCC-112 protein (SCC-112), TGCATTGATAGGGACCTTTGTCTCTTCCTCCC mRNA TTTGATTAATTGCCCGGCATCACAGTTT (SEQ ID NO: 246) 4 A_24_P649624 BC063684 Homo sapiens cDNA clone IMAGE: 4395035, CTGTTAGAGCCAAAATTGTGATGAGCAATACT partial cds. GATAATTGTCCAGTTTATGTCATCTTTC (SEQ ID NO: 247) 4 A_24_P6921 NM_052871 MGC4677 Homo sapiens hypothetical protein MGC4677 CAGGAAGCTCTATGACACACTTGATCGAATAT (MGC4677), mRNA GACAGACACTGAAAATCACGACTCATCC (SEQ ID NO: 248) 4 A_24_P759747 CNS01RGE Human chromosome 14 DNA sequence BAC R- GGAGGAGCCCCACCTTCTGCTACTATTATGTT 300J18 of library RPCI-11 from chromosome 14 of CTTCAGATGAGTAGAAGAGAGTGGGGAG Homo sapiens (Human), complete sequence. (SEQ ID NO: 249) 4 A_24_P8151 AK098403 Homo sapiens cDNA FLJ25537 fis, clone ATCTAGCAGGCGACTGAGTGCCGAGAAAATAC CBR09136. CTGGCAGAGGTGGGCACAAGGCGGGGTC (SEQ ID NO: 250) 4 A_24_P86389 NM_003514 HIST1H2AM Homo sapiens histone 1, H2am (HIST1H2AM), CTTGGTAAAGTTACCATCGCTCAGGGCGGTGT mRNA TCTGCCTAACATCCAGGCCGTACTGCTC (SEQ ID NO: 251) 4 A_32_P112452 NM_002965 S100A9 Homo sapiens S100 calcium binding protein A9 CGTGGGAGGTGTTGATGATGGTCTCTATGTTG (calgranulin B) (S100A9), mRNA CGTTCCAGCTGCGACATTTTGCAAGTCA (SEQ ID NO: 252) 4 A_32_P113646 NM_005544 IRS1 Homo sapiens insulin receptor substrate 1 (IRS1), CAGTCTCTTCCTCTCTGGGAGCTGGCTGGAG mRNA CTGGGATGGACACCTGACAGAAGGAAATT (SEQ ID NO: 253) 4 A_32_P143589 AC018758 CD177 Homo sapiens chromosome 19, BAC CTB-61I7 AGCTTGGATGGTAGCAGAGACTTCAGGGTGC (BC52850), complete sequence. TCCAGCCAAACGTATTTGGGCATCACCAT (SEQ ID NO: 254) 4 A_32_P146815 AC007528 Homo sapiens 12 BAC RP11-473N11 (Roswell TACCTTTTGCATATGCTTTTCTTGGCCTTAGGA Park Cancer Institute Human BAC Library) TAGTACTGGACTTTGTTGTCCTCTGCT (SEQ ID complete sequence. NO: 255) 4 2 Granulocyte A_32_P198223 AC022784 Homo sapiens chromosome 8, clone RP11-10A14, CAGGAATCACGGGAGTGAATCACATTCCAGAC complete sequence. ACTTGCTTGGACTTCATCACATCCTCAG (SEQ ID NO: 256) 4 26 Granulocyte A_32_P228455 AC073172 Homo sapiens chromosome 11, clone RP11- AGTTACTTGCCTCCAGATATCTTGGTGTGTGA 531H8, complete sequence. GAACATTAAATCTGTATGTGTCTAAATC (SEQ ID NO: 257) 4 A_32_P41604 HS86F14 Human DNA sequence from clone RP1-86F14 on GATCTGGAAAATACTTGTTTGGGGATCAATAAT chromosome 1q23-24 Contains the F5 gene for ATGTTTGGGCTATTATCTAATGCTGTG (SEQ ID coagulation factor V (proaccelerin NO: 258) labile factor) and the 3′ end of the SELP gene for selectin P (granule membrane protein 140 kDa antigen CD62), complete sequence. 4 A_32_P47754 HSM803756 Homo sapiens mRNA; cDNA DKFZp434F1129 TTCACGTCAACTTCTGGCTCCTCAGTTTGGCA (from clone DKFZp434F1129). GTAAGGCAGGGAAGTTGTTTTCCTATTT (SEQ ID NO: 259) 4 A_32_P9753 AC004686 Homo sapiens chromosome 17, clone ATTGGATAGGAAGAGGAATAAAATATAAAAATC hRPC.1073_F_15, complete sequence. AGAGAACTGCTGAAATTCTGTGACCCC (SEQ ID NO: 260) 5 Platelet 5 A_23_P104624 XM_290546 KIAA0830 PREDICTED: Homo sapiens KIAA0830 protein, GGAGAGAACACATGGTACAATCGTAACACATG transcript variant 1 (KIAA0830), mRNA AAGGACAAGTAAGTGCTGCAGTAAAGGT (SEQ ID NO: 261) 5 A_23_P118313 NM_007285 GABARAPL2 Homo sapiens GABA(A) receptor-associated TGAGGTAGGTGCGGTATTAAAGTGAAAGGGAA protein-like 2 (GABARAPL2), mRNA GGTGATGCATTTATTCTGGGTTATGCTT (SEQ ID NO: 262) 5 A_23_P131646 NM_144563 RPIA Homo sapiens ribose 5-phosphate isomerase A ACTTTTGCTAAGATCTGGGGGTTTCTTCATATT (ribose 5-phosphate epimerase) (RPIA), mRNA CCTGCTGTTGGAAGCAGTTGACCAGAA (SEQ ID NO: 263) 5 A_23_P134925 NM_004331 BNIP3L Homo sapiens BCL2/adenovirus E1B 19 kDa ATTTGGGGACAAAAAGGCAGGCTTCATTTTTC interacting protein 3-like (BNIP3L), mRNA ATATGTTTGATGAAAACTGGCTCAAGAT (SEQ ID NO: 264) 5 A_23_P137434 NM_014372 RNF11 Homo sapiens ring finger protein 11 (RNF11), TGTAGTATCCATATGTTGCTTAAATTTCCTTAT mRNA GAGCCCCATGATGGAAAGACTTAAAGA (SEQ ID NO: 265) 5 A_23_P140256 NM_000270 NP Homo sapiens nucleoside phosphorylase (NP), CTACTAGCTCTTTGAGATAATACATTCCGAGG mRNA GGCTCAGTTCTGCCTTATCTAAATCACC (SEQ ID NO: 266) 5 A_23_P141764 NM_003826 NAPG Homo sapiens N-ethylmaleimide-sensitive factor CATGCCATTTCAAGGACTTGGGAATAGATTAG attachment protein, gamma (NAPG), mRNA GGATATCCGTACTTCATTACAGTCATGA (SEQ ID NO: 267) 5 A_23_P144145 AC092953 Homo sapiens 3 BAC RP11-531F16 (Roswell Park TCTTTAGTGAATATCATCTGCATATCTCTGTAA Cancer Institute Human BAC Library) complete GTTCAATTGTGTTTCTTACAGTCCCTG (SEQ ID sequence. NO: 268) 5 A_23_P145114 NM_001498 GCLC Homo sapiens glutamate-cysteine ligase, catalytic AGAATGCCTGGTTTTCGTTTGCAATTTGCTTGT subunit (GCLC), mRNA GTAAATCAGGTTGTAAAAAGGCAGATA (SEQ ID NO: 269) 5 2 Platelet A_23_P157795 NM_003798 CTNNAL1 Homo sapiens catenin (cadherin-associated GGATAGTAAAACTTGAGAAGCTTTTGGGGTCA protein), alpha-like 1 (CTNNAL1), mRNA GATCTCTGGAACATCATGTGATGAAGCT (SEQ ID NO: 270) 5 A_23_P160359 NM_004437 EPB41 Homo sapiens erythrocyte membrane protein band AGAGCAAGAGCAGTATGAAAGTACCATCGGAT 4.1 (elliptocytosis 1, RH-linked) TCAAACTTCCCAGTTACCGAGCAGCTAA (SEQ (EPB41), transcript variant 3, mRNA ID NO: 271) 5 A_23_P203558 NM_000518 HBB Homo sapiens hemoglobin, beta (HBB), mRNA GTCCAACTACTAAACTGGGGGATATTATGAAG GGCCTTGAGCATCTGGATTCTGCCTAAT (SEQ ID NO: 272) 5 A_23_P209426 NM_015049 TRAK2 Homo sapiens trafficking protein, kinesin AGAAAATGTTGTGCTGTATGTTCTTGATTTGAC binding 2 (TRAK2), mRNA ATAAATGAATAGACTTTGGCAAGGGAG (SEQ ID NO: 273) 5 A_23_P21785 NM_022072 NSUN3 Homo sapiens NOL1/NOP2/Sun domain family, ACGGTAACATCATGCCTATGGACATTAAAGGA member 3 (NSUN3), mRNA ATAGCAAGGACTTGCTCCCACGACTTCA (SEQ ID NO: 274) 5 A_23_P383377 NM_006563 KLF1 Homo sapiens Kruppel-like factor 1 (erythroid) GGACCCGGGACGGTGGGCACTGGACTCGGG (KLF1), mRNA GGGACTGCAGAGGATCCAGGTGTGATAGCC (SEQ ID NO: 275) 5 A_23_P38757 NM_015865 SLC14A1 Homo sapiens solute carrier family 14 (urea GTATTAAAAATTAAACCCCCATAAACCCAACCT transporter), member 1 (Kidd blood group) AAGCCTATGGAATCCACAGTCACAAAAA (SEQ (SLC14A1), mRNA ID NO: 276) 5 A_23_P397999 NM_003468 FZD5 Homo sapiens frizzled homolog 5 (Drosophila) GGGGCTTTACAATCCTAAGGTTGGCGTTGTAA (FZD5), mRNA TGAAGTTCCACTTGGTTCAGGTTTCTTT (SEQ ID NO: 277) 5 2 Platelet A_23_P45304 NM_021083 XK Homo sapiens X-linked Kx blood group (McLeod GCTTTCGTTGACTGCTTCTCTGCAGTCGTTGA syndrome) (XK), mRNA TGCTAATAAATATTGTCCTGTTTCTTCA (SEQ ID NO: 278) 5 A_23_P55578 NM_003831 RIOK3 Homo sapiens RIO kinase 3 (yeast) (RIOK3), CTTTAGTGGGTAGAACAAATGGAAATTTGGTTT transcript variant 1, mRNA CAGAATGGCTGACAGAAATCGACATAA (SEQ ID NO: 279) 5 A_23_P60324 NM_016172 UBADC1 Homo sapiens ubiquitin associated domain TTTAGCATCTGACAGGTGTTTACAAAAAAGTG containing 1 (UBADC1), mRNA GTTGTCGCACTGGGAAGTGGAGTGATGG (SEQ ID NO: 280) 5 A_23_P63547 XM_931256 CR1L PREDICTED: Homo sapiens complement AACACCTGTTTGTGACAGTGAGTTGAAATATG component (3b/4b) receptor 1-like, transcript CATTCCTATTTCTTTTACCGATACATTC (SEQ ID variant 3 (CR1L), mRNA NO: 281) 5 A_23_P67708 NM_003200 TCF3 Homo sapiens transcription factor 3 (E2A CGGAGAAATGGAAACATATCACTCAAGGGGGA immunoglobulin enhancer binding factors TGCTGTGGAAACCTGGCTTATTCTTCTA (SEQ E12/E47) (TCF3), mRNA ID NO: 282) 5 A_23_P69695 NM_001008388 LOC493856 Homo sapiens similar to RIKEN cDNA ATTTGTGTCTTACTAAAGCAGCTTATTGTAGGT 1500009M05 gene (LOC493856), mRNA GTTGGCGTTCTAAAACGTTTCCTGCCT (SEQ ID NO: 283) 5 A_23_P70843 NM_001724 BPGM Homo sapiens 2,3-bisphosphoglycerate mutase TAGTAGAATTCCTCTTTGGCCACAAGAATAAG (BPGM), transcript variant 1, mRNA CAGCAAATAAACAACTATGGCTGTTGAG (SEQ ID NO: 284) 5 A_24_P132039 NM_004290 RNF14 Homo sapiens ring finger protein 14 (RNF14), GGGTGTTAGAACCTAGATTCAAAATGGCTTGT transcript variant 1, mRNA CTTTGCTACTTTTGTTCCACATTCTCTC (SEQ ID NO: 285) 5 A_24_P173823 HSM800166 Homo sapiens mRNA; cDNA DKFZp586J2118 ATGATACTAACACGGTGTAGGTTTTACAGTCTC (from clone DKFZp586J2118). CTAATTTGTACTGGTAATGCATATTCC (SEQ ID NO: 286) 5 A_24_P285880 NM_003262 TLOC1 Homo sapiens translocation protein 1 (TLOC1), AAGGTATTTTTCCTTTTCCCTCTTACTGGATTT mRNA TTCAATTTTCAAACCATATGGCCTAGG (SEQ ID NO: 287) 5 A_24_P32790 NM_018566 YOD1 Homo sapiens YOD1 OTU deubiquinating enzyme CTAGGGATCTAATTAAGGACATTAAAGTACAAT 1 homolog (yeast) (YOD1), mRNA TCTTGAGCTACTAACCATCAGCTCTTC (SEQ ID NO: 288) 5 A_24_P335620 NM_003486 SLC7A5 Homo sapiens solute carrier family 7 (cationic TTTCAGTCGTTGTGCTTTTTTGTTTTGTGCTAA amino acid transporter, y+ system), member 5 CGTCTTACTAATTTAAAGATGCTGTCG (SEQ ID (SLC7A5), mRNA NO: 289) 5 A_24_P483083 NM_007111 TFDP1 Homo sapiens transcription factor Dp-1 (TFDP1), AAACAGAAACAGTCTCAACTTCAAAACTTATTC mRNA TACAGCAAATTGCCTTCAAGAACCTGG (SEQ ID NO: 290) 5 A_24_P503866 XM_930101 LOC647087 PREDICTED: Homo sapiens hypothetical protein TATACCTTTTCACATTAAAAAAGGTATTTATATT LOC647087 (LOC647087), mRNA ATTACTTTGTAGTGATTGTCTTAAGA (SEQ ID NO: 291) 5 A_24_P570806 TCTCAGAAGACAGAGGGTTTTCTTTTGAGGTA AATTTGATAGTACATTTTGATAGTACGG (SEQ ID NO: 292) 5 A_24_P599496 CNS01DVX Human chromosome 14 DNA sequence BAC C- GGCGGAAAACAAGTTTAGTCACAGAAGACTAC 2555C10 of library CalTech-D from chromosome TCCATGTTTGAGCTTCTGTTTCAAGGGA (SEQ 14 of Homo sapiens (Human), complete ID NO: 293) sequence. 5 A_24_P673786 AL513128 Human DNA sequence from clone RP11-301N24 GTCTATAACAAACAGTCTGTTCATTTATTTCTG on chromosome 10 TTGATAAACCATTTGGACAGAGTGAGG (SEQ ID NO: 294) 5 A_24_P67946 NM_019094 NUDT4 Homo sapiens nudix (nucleoside diphosphate GAACTCAGATTTGCAAACCAGGTTTCTGAAAC linked moiety X)-type motif 4 (NUDT4), transcript TTTGGGTAAGGTGTATGCTTTTAACTTT (SEQ variant 1, mRNA ID NO: 295) 5 A_24_P886515 AC124287 Homo sapiens chromosome 17, clone RP13- CGTTGCCTGTCTTGCTGGATAACTGCATATATT 991F5, complete sequence. GTGTTCAGTTGTGTATTTGTTTTGCTT (SEQ ID NO: 296) 5 A_24_P926507 AC087685 Homo sapiens chromosome 18, clone RP11- GAATAAACAGAAATAGGGAAGTAAACCTACAA 618K16, complete sequence. ATATTTTAGGGAGAAGCTCACTTCTTCC (SEQ ID NO: 297) 5 A_24_P935893 NM_017709 FAM46C Homo sapiens family with sequence similarity 46, TTCACATGCAAGTTCTAATCTAAAGTTAAGCAG member C (FAM46C), mRNA TCTCTTATTTGTTTCGGGACTCTGATT (SEQ ID NO: 298) 5 4 Platelet A_32_P109653 AF163864 Homo sapiens SNCA isoform (SNCA) gene, TGTGGTTTGGTATTCCAAGTGGGGTCTTTTTC complete cds, alternatively spliced. AGAATCTCTGCACTAGTGTGAGATGCAA (SEQ ID NO: 299) 5 A_32_P11181 AC034102 Homo sapiens 12 BAC RP11-603J24 (Roswell GGCATGCTGTCCCAGGAAACTAGGGCTCCCA Park Cancer Institute Human BAC Library) CTAACTTATGAGGTTTTTAAACACATTGA (SEQ complete sequence. ID NO: 300) 5 A_32_P122715 AC025300 Homo sapiens chromosome 11, clone RP11- GAAAGTTCACATACAGGGGAAAGTGTACGATT 573E11, complete sequence. TCATCTACTGTTTATCTTCTAACCTCAC (SEQ ID NO: 301) 5 A_32_P133840 NM_014858 TMCC2 Homo sapiens transmembrane and coiled-coil CTTCCATTCCATTTAGCCTTTGGATCATCCTGG domain family 2 (TMCC2), mRNA CTGGGAGAAGTGGGACCGAGCCACCCA (SEQ ID NO: 302) 5 A_32_P159651 NM_003884 PCAF Homo sapiens p300/CBP-associated factor GAGTGGTGTCTAGATTTCTAATGAAGAATCAT (PCAF), mRNA GATACAGTTTGGATTAAGTATCTTGGAC (SEQ ID NO: 303) 5 A_32_P165297 HSJ842K24 Human DNA sequence from clone RP5-842K24 on GAGGGGTATTTAGGGCCACTGTATTTTTGGTG chromosome Xq25-26.3 Contains the 3′ end of the CCACAATTTTCTACATTGTTGGCATTTT (SEQ MBNL3 gene for muscleblind-like 3 (Drosophila) ID NO: 304) and a novel gene, complete sequence. 5 A_32_P1712 NM_002934 RNASE2 Homo sapiens ribonuclease, RNase A family, 2 TCCAGGTGCCTTTAATGTACTGTAACCTCACAA (liver, eosinophil-derived neurotoxin) (RNASE2), CTCCAAGTCCACAGAATATTTCAAACT (SEQ ID mRNA NO: 305) 5 A_32_P175183 AC019227 ZBTB44 Homo sapiens BAC clone RP11-567O18 from 11, CAGTCAAGCTGTGGATGAAATGACCAGGAACG complete sequence. GAGAATGAAGTATGTAAATCCCAGCTTC (SEQ ID NO: 306) 5 A_32_P178945 NM_018566 YOD1 Homo sapiens YOD1 OTU deubiquinating enzyme TTGCCAGCATTTTTTGAAGTAATACACTGCTGC 1 homolog (yeast) (YOD1), mRNA TACCTGGAAGATGTCTAACTTCATTTT (SEQ ID NO: 307) 5 A_32_P192480 HSJ842K24 Human DNA sequence from clone RP5-842K24 on TAGTGCTGTAGTGCTTGTTTATGTTTAAAAGTG chromosome Xq25-26.3 Contains the 3′ end of the CACATTATGCAGCTCATTTTAGTATGC (SEQ ID MBNL3 gene for muscleblind-like 3 (Drosophila) NO: 308) and a novel gene, complete sequence. 5 A_32_P204048 HSJ842K24 Human DNA sequence from clone RP5-842K24 on GGGTGGGAAAGCATAAGATGGGGACTAAGAC chromosome Xq25-26.3 Contains the 3′ end of the TTTGCCTTTAACCTTCATGACATGAAGAA (SEQ MBNL3 gene for muscleblind-like 3 (Drosophila) ID NO: 309) and a novel gene, complete sequence. 5 A_32_P23795 XM_929854 LOC646890 PREDICTED: Homo sapiens hypothetical protein GATGAAGAATTTGCCTTACTTTGTTGTTCGCTC LOC646890 (LOC646890), mRNA AGTTCCTAAGACTGTGAGTTGTCAAAT (SEQ ID NO: 310) 5 A_32_P36694 NM_175061 JAZF1 Homo sapiens juxtaposed with another zinc finger CAGGTAAGGATGGGAATATTTTGTTATACTGT gene 1 (JAZF1), mRNA GTATAGTGAATGTATTGTACTGTGTCTG (SEQ ID NO: 311) 5 A_32_P465742 NM_001031687 PIP5K1B Homo sapiens phosphatidylinositol-4-phosphate 5- TTCCTATGGACTTTTGCATTATTTCATTGTGCA kinase, type I, beta (PIP5K1B), TGCATCCAGTGATTATACATAAGCAAC (SEQ ID transcript variant 1, mRNA NO: 312) 6 all cell types 6 A_23_P109133 NM_000490 AVP Homo sapiens arginine vasopressin (neurophysin CGAGAGCTGCGTGACCGAGCCCGAGTGCCGC II, antidiuretic hormone, diabetes insipidus, GAGGGCTTTCACCGCCGCGCCCGCGCCAG neurohypophyseal) (AVP), mRNA (SEQ ID NO: 313) 6 A_23_P15174 NM_005949 MT1F Homo sapiens metallothionein 1F (functional) TGCCAGGACAACCTTTCTCCCAGATGTAAACA (MT1F), mRNA GAGAGACATGTACAAACCTGGATTTTTT (SEQ ID NO: 314) 6 A_23_P157943 NM_016219 MAN1B1 Homo sapiens mannosidase, alpha, class 1B, AGCTATGACAACAGCAAGAGTTGGCGGCGGC member 1 (MAN1B1), mRNA GCTCGTGCTGGAGGAAATGGAAGCAACTG (SEQ ID NO: 315) 6 A_23_P159191 NM_000805 GAST Homo sapiens gastrin (GAST), mRNA AGCCTATGGATGGATGGACTTCGGCCGCCGC AGTGCTGAGGATGAGAACTAACAATCCTA (SEQ ID NO: 316) 6 A_23_P16483 NM_000455 STK11 Homo sapiens serine/threonine kinase 11 CCGTGGCCTCGTGCTCCGCAGGGCGCCCAGC (STK11), mRNA GCCGTCCGGCGGCCCCGCCGCAGACCAGC (SEQ ID NO: 317) 6 A_23_P208900 GGGTCTCCGAGGTGCCGGTTAGGAGTTTGAA CCCCCCCCACTCTGCAGAGGGAAGCGGGG (SEQ ID NO: 318) 6 A_23_P211345 NM_080647 TBX1 Homo sapiens T-box 1 (TBX1), transcript variant TGTAGATACTGTAGATACTGTAGATACCGCCC C, mRNA CGGCGCCGACTTGATAAACGGTTTCGCC (SEQ ID NO: 319) 6 A_23_P25790 NM_022478 CDH24 Homo sapiens cadherin-like 24 (CDH24), CGAGACGTGTTGCCCCGGGCCCGGGTGTCGC transcript variant 1, mRNA GCCAGCCCAGACCCCCCGGCCCCGCCGAC (SEQ ID NO: 320) 6 A_23_P3413 NM_130901 OTUD7 Homo sapiens OTU domain containing 7 GCCGACGCGCCGACCGCGCGCTCGAACGGT (OTUD7), mRNA GAGTGCGGCCGTGGCGGCCCGGGGCCGGTG (SEQ ID NO: 321) 6 A_23_P346309 NM_004324 BAX Homo sapiens BCL2-associated X protein (BAX), CCCGCGCGGACCCGGCGAGAGGCGGCGGCG transcript variant beta, mRNA GGAGCGGCGGTGATGGACGGGTCCGGGGAG (SEQ ID NO: 322) 6 A_23_P35534 NM_020999 NEUROG3 Homo sapiens neurogenin 3 (NEUROG3), mRNA CATTCAAAGAATACTAGAATGGTAGCACTACC CGGCCGGAGCCGCCCACCGTCTTGGGTC (SEQ ID NO: 323) 6 A_23_P401626 NM_174919 LOC201175 Homo sapiens hypothetical protein LOC201175 GCAGCGACTCAGAGAACGTCTACGAGGTCAT (LOC201175), mRNA CCAGGACTTGCACGTCCCGCCGCCGGAGG (SEQ ID NO: 324) 6 A_23_P431346 NM_175887 LOC222171 Homo sapiens hypothetical protein LOC222171 CCCCAAACCAGACAAGTTATACGGGGACAAAT (LOC222171), mRNA CCGGCAGCAGCCGCCGCAATTTGAAGAT (SEQ ID NO: 325) 6 A_23_P96072 NM_000832 GRIN1 Homo sapiens glutamate receptor, ionotropic, N- CAGGGTGCAGGCGCGCACCGCCCAACCCCCA methyl D-aspartate 1 (GRIN1), transcript variant CCTCCCGGTGTATGCAGTGGTGATGCCTA NR1-1, mRNA (SEQ ID NO: 326) 6 A_24_P108738 NM_153334 SCARF2 Homo sapiens scavenger receptor class F, CAGCGCCGCTGCAGCTGGCCGTGCGCCCTCA member 2 (SCARF2), transcript variant 1, mRNA CCACCGCCGCCAGGCTCCGAGGCCGCGCC (SEQ ID NO: 327) 6 A_24_P112803 NM_005986 SOX1 Homo sapiens SRY (sex determining region Y)- GCTGGGCTCTCTGGTGAAGTCGGAGCCCAGC box 1 (SOX1), mRNA GGCAGCCCGCCCGCCCCAGCGCACTCGCG (SEQ ID NO: 328) 6 A_24_P113725 NM_005634 SOX3 Homo sapiens SRY (sex determining region Y)- GCCGCCCGCCATCGCATCGCACTCTCAGCGC box 3 (SOX3), mRNA GCGTGCCTCGGCGACCTGCGCGACATGAT (SEQ ID NO: 329) 6 A_24_P11737 XR_015426 LOC731268 PREDICTED: Homo sapiens similar to zinc finger GTGAGAAGTTCTGCAGATGTATGTGGCGCACA protein 499 (LOC731268), GCCTCTACAGCCGCCGACTCCGACTCCT (SEQ ID NO: 330) 6 A_24_P117782 NM_033129 SCRT2 Homo sapiens scratch homolog 2, zinc finger CTTCAAGCACTACCGCTGCCGCCAGTGCGAC protein (Drosophila) (SCRT2), mRNA AAGAGCTTCGCGCTCAAGTCCTACCTCCA (SEQ ID NO: 331) 6 A_24_P127719 NM_201589 MAFA Homo sapiens v-maf musculoaponeurotic GTTCGAGGTGAAGAAGGAGCCTCCCGAGGCC fibrosarcoma oncogene homolog A (avian) GAGCGCTTCTGCCACCGCCTGCCGCCAGG (MAFA), mRNA (SEQ ID NO: 332) 6 A_24_P144465 NM_022107 GPSM3 Homo sapiens G-protein signalling modulator 3 CAGACTGAACTCCTTCTGGACCTGGTGGCTGA (AGS3-like, C. elegans) (GPSM3), mRNA AGCCCAGTCCCGCCGCCTGGAGGAGCAG (SEQ ID NO: 333) 6 A_24_P253293 NM_014360 NKX2-8 Homo sapiens NK2 transcription factor related, GCGAGGTGGGAACCGCCGCGGCCCAGGAGA locus 8 (Drosophila) (NKX2-8), mRNA AGTGCGGCGCCCCTCCAGCCGCCGCCTGCC (SEQ ID NO: 334) 6 A_24_P273378 NM_006549 CAMKK2 Homo sapiens calcium/calmodulin-dependent CCGGGCCGCCCCCCAGGATGAGCTGGGGGG protein kinase kinase 2, beta (CAMKK2), TAGGGGCAGCAGCAGCAGCGAAAGCCAGAA transcript variant 1, mRNA (SEQ ID NO: 335) 6 A_24_P280660 NM_178174 TREML1 Homo sapiens triggering receptor expressed on GAGGGGTGCCAGCCCCTGGTGTCCTCAGCTG myeloid cells-like 1 (TREML1), mRNA TGGATCGCAGAGCTCCAGCGGGCAGGCGT (SEQ ID NO: 336) 6 A_24_P315500 NM_014223 NFYC Homo sapiens nuclear transcription factor Y, TCAGGAGTCCAGGAAGAGCAGGAGCCGCCCC gamma (NFYC), mRNA CGCGCTCCTACGGAGTCGGGCAATGCAGA (SEQ ID NO: 337) 6 A_24_P328446 NM_016170 TLX2 Homo sapiens T-cell leukemia homeobox 2 ACGGAGCCTCGGGCTACGGTCCCGCCGGCTC (TLX2), mRNA ACTTGCCCCGCTGCCCGGCAGCTCCGGAG (SEQ ID NO: 338) 6 A_24_P376451 NM_000514 GDNF Homo sapiens glial cell derived neurotrophic AACAGCAATGGTGCCGCCGCCGGACGGGACT factor (GDNF), transcript variant 1, mRNA TTAAGATGAAGTTATGGGATGTCGTGGCT (SEQ ID NO: 339) 6 A_24_P37665 NM_022042 SLC26A1 Homo sapiens solute carrier family 26 (sulfate TTATTTGAACAAGGGTCCCCCGCCATCATGCA transporter), member 1 (SLC26A1), transcript GCCTCCAAGGTGCCAAGAGGACTCCCTA (SEQ variant 1, mRNA ID NO: 340) 6 A_24_P40775 XM_290842 LRFN1 PREDICTED: Homo sapiens leucine rich repeat AGGGGGCGCGGCCGGGGAGGATGGAGACCT and fibronectin type III domain containing 1 GGGGCTGGGCTCCGCCAGGGCGTGCCTGGC (LRFN1), mRNA (SEQ ID NO: 341) 6 A_24_P416595 NM_174945 ZNF575 Homo sapiens zinc finger protein 575 (ZNF575), CAAGCTGGCCACGCACCGCTTAGCACACGGA mRNA GGCGCCCGACCCCACCCATGCCCAGACTG (SEQ ID NO: 342) 6 A_24_P471099 TGCAGGTTTTTGCCCCCGCCGTTGCGGCTGTT TTCCCCCCGTCAGCGAGGCTTTTTGTTG (SEQ ID NO: 343) 6 A_24_P535483 NM_207349 LOC284739 Homo sapiens hypothetical protein LOC284739 AGGAGGCCCGCCCTCCACGCGCCGAAGGCCT (LOC284739), mRNA CAATAAACGGAGCTGGCGCTGCGGGTCCG (SEQ ID NO: 344) 6 A_24_P600087 GGGGGTTTCCCCCCCGGGAGGACCCCCCCTG GGGGCCCCCCTGTTTGTTACACGGCGGGT (SEQ ID NO: 345) 6 A_24_P75183 NM_199046 TEPP Homo sapiens testis/prostate/placenta-expressed TCAGCGGCTACGCGGTGCGGTACTTGAAGCC protein, isoform 2 (TEPP), transcript variant 1, CGACGTGACCCAGACCTGGCGGTACTGCC mRNA (SEQ ID NO: 346) 6 A_24_P780709 AGGCAGCCGCCGGGCCAGGTCGAGGCCGCC GCCGCCCGGCCAGAGCACGCCAGGGAGCAG (SEQ ID NO: 347) 6 A_24_P920135 CAAGTGGAAAAAAATATTAAAAAACTGATAATG GCCTCGGTTGGCCTCAGCGGCGGAACT (SEQ ID NO: 348) 6 A_32_P138359 NM_012331 MSRA Homo sapiens methionine sulfoxide reductase A TGCGGCTCCGCTGCCGGTAGCGCCGTCCCCC (MSRA), mRNA GGGACCACCCTTCGGCTGGCGCCCTCCCA (SEQ ID NO: 349) 6 A_32_P336712 NM_173573 C11orf35 Homo sapiens chromosome 11 open reading AGCCCCAAGGGCGAGGTCCTCAGTGAGCACC frame 35 (C11orf35), mRNA GGATCCCACGCCGCGAGACTCCGGCCCCG (SEQ ID NO: 350) 6 A_32_P509169 NM_207322 NLF1 Homo sapiens nuclear localized factor 1 (NLF1), CCCCGCCTGGCCTTGGCTGCGCTCCGGAATT mRNA CTTGGGTCGAAGAAGCAGGGATGGACGAG (SEQ ID NO: 351) 7 B cells 7 4 B cells A_23_P158817 NM_001040070 ELK2P1 ELK2, member of ETS oncogene family, ATGCATGAGGCTCTGCACAACCACTACACGCA pseudogene 1 GAAGAGCCTCTCCCTGTCTCCGGGTAAA (SEQ ID NO: 352) 7 4 B cells A_23_P158868 ACACCTTCTACGGTATGGACGTCTGGGGCCAA GGGACCACGGTCACCGTCTCCTCAGCAT (SEQ ID NO: 353) 7 A_23_P168229 NM_022085 TXNDC5 Homo sapiens thioredoxin domain containing 5 ATACGCAAGGGGATGTGGATACTTGGCCCAAA (TXNDC5), transcript variant 2, mRNA GTAACTGGTGGTAGGAATCTTAGAAACA (SEQ ID NO: 354) 7 7 B cells A_23_P21260 TAGGAGACAGAGTCACCATCACTTGCCGGGC AAGTCAGACCATTAGCAGCTATTTAAATT (SEQ ID NO: 355) 7 4 B cells A_23_P350782 XM_942302 LOC652694 PREDICTED: Homo sapiens similar to Ig kappa GCAGCCTGCAGCCTGAAGATATTGCAACATAT chain V-I region HK102 precursor (LOC652694), TACTGTCAACAGTATGATAATCTCCCTC (SEQ mRNA ID NO: 356) 7 5 B cells A_23_P361654 AC073416 Homo sapiens BAC clone RP11-136K15 from 2, TCAGGGTATTAGCAGCTGGTTAGCCTGGTATC complete sequence. AGCAGAAACCAGAGAAAGCCCCTAAGTC (SEQ ID NO: 357) 7 9 B cells A_23_P435390 AGACAGCACTGGTTCTTATTTGCTGTTCGGCG GAGGGACCAAGCTGACCGTCCTAGGTCA (SEQ ID NO: 358) 7 3 B cells A_23_P44053 AGCTCCTGATCTACGATGCATCCACTTTGGAA ACCGGGGTCCCATCAAGGTTCAGTGCAC (SEQ ID NO: 359) 7 7 B cells A_23_P61042 S55735 Homo sapiens immunoglobulin A1-A2 lambda GAGTTGAAGACCCCACTAACCGCCAACATCAC hybrid GAU heavy chain mRNA, partial cds. AAAATCCGGAAACACATTCCGGCCCGAG (SEQ ID NO: 360) 7 8 B cells A_23_P61068 GCCTGAAGATCTTGCAGTATATTACTGTCAGC AGTATAGTAGTCCACCTCGGACTTTTGG (SEQ ID NO: 361) 7 A_23_P72330 AGATGGTGCAGCCACAGTTCGTTTGATCTCCA GCTCGAGCCGCTGCGTGTTTTCCTCTTG (SEQ ID NO: 362) 7 5 B cells A_23_P84596 NM_016459 PACAP Homo sapiens proapoptotic caspase adaptor GGACATGTTTGCACTACTTGGGGGAGTTTGGA protein (PACAP), mRNA GAAGACCAGATCTATGAAGCCCACCAAC (SEQ ID NO: 363) 7 4 B cells A_24_P100684 ATGGTATGATGGAAGTAATAAATACTATGCAGA CTCCGTGAAGGGCCGATTCACCATCTC (SEQ ID NO: 364) 7 5 B cells A_24_P144346 GTGGCACATACTATGCAGACTCCGTGAAGGG CCGATTCACCATCTCCAGAGACAATGCCA (SEQ ID NO: 365) 7 6 B cells A_24_P15388 GCCAAGAACACGCTGTATCTGCAAATGAACAG TCTGAGAGCCGAGGACACGGCTGTGTAT (SEQ ID NO: 366) 7 2 B cells A_24_P15550 GCAGGGTGGAGGCTGAGGATGTTGGGGTTTA TTACTGCATGCAAGGTACACACTGGCCTC (SEQ ID NO: 367) 7 A_24_P169713 S80758 Ig VL = platelet glycoprotein IIIa CATAGTTATAACCAACGTCACTGCTGGTT leucine-33 form-specific antibody light CCAGTGCAGGAGATGGTGATCGACTGTC (SEQ chain variable region [human, ID NO: 368) plasma, mRNA Partial, 329 nt]. 7 13 B cells A_24_P169873 HSM806780 Homo sapiens mRNA; cDNA DKFZp686O16217 GTAAACCCACCCACATCAATGTGTCTGTTGTC (from clone DKFZp686O16217). ATGGCGGAGGCGGATGGCACCTGCTACT (SEQ ID NO: 369) 7 A_24_P204374 AGCCTGATGCCTGAACAGTGGAGATCCCGCA GCAGCTACAACTGCTGGGCCATGCATAAA (SEQ ID NO: 370) 7 4 B cells A_24_P204574 HUMIGLVE Homo sapiens Ig germline lambda-chain gene GAGGATGAGGCTGATTATTACTGTGCAGCATG variable region myeloma subgroup I (IGLV), GGATGACAGCCTGAGTGGTCCCACAGTG complete exon. (SEQ ID NO: 371) 7 5 B cells A_24_P212024 TGATCTATGCTGCATCCAGTTTGCAGTCGGGG GTCCCATCTCGGTTCAGTGGCAGTGGAT (SEQ ID NO: 372) 7 5 B cells A_24_P239076 NM_001013618 LOC91353 Homo sapiens similar to omega protein AACAAGGCCACACTGGTGTGTCTCATGAATGA (LOC91353), mRNA CTTCTATCTGGGAATCTTGACGGTGACC (SEQ ID NO: 373) 7 4 B cells A_24_P24371 CACAAGCCCAGCAACACCAAGGTGGACAAGA GAGTTGAGTCCAAATATGGTCCCCCATGC (SEQ ID NO: 374) 7 7 B cells A_24_P272146 TCACTATCAGCAGCCTGCAGCCTGAAGATTTT GCAACTTACTATTGTCAACAGGCTAACA (SEQ ID NO: 375) 7 3 B cells A_24_P315854 ATCAGTAGACACGTCCAAGAACCAGTTCTCCC TGAAGCTGAGCTCTGTGACCGCTGCGGA (SEQ ID NO: 376) 7 4 B cells A_24_P33341 XM_370973 LOC388255 PREDICTED: Homo sapiens similar to Ig heavy CCGTATCTGCAAATGAACAGCTTGAGAGCTGA chain V-III region VH26 precursor (LOC388255), GGACACGGCTGTGTATTACTGTGTGAAA (SEQ mRNA ID NO: 377 7 7 B cells A_24_P357847 CCATCAGCAGCCTGCAGTCTGAAGATTTTGCA GTTTATTACTGTCAGCAGTATAATAACT (SEQ ID NO: 378) 7 4 B cells A_24_P465799 AF063695 Homo sapiens clone BCPBLL11 immunoglobulin CTGTCAGGTGTGGGATAGTACTAGTGATCATT lambda light chain variable region mRNA, partial ATGTCTTCGGAACTGGGACCAAGGTCGC (SEQ cds. ID NO: 379) 7 6 B cells A_24_P488083 HSA519285 Homo sapiens partial mRNA for IgM CAATTCCAAGAACACGCTGTATCTGCAAGTGA immunoglobulin heavy chain variable region (IGHV ACAGCCTGAGAGTCGAGGACACGGCCCT gene), clone ANBPM204. (SEQ ID NO: 380) 7 6 B cells A_24_P490109 AGCAGCCTGCAGCCTGAAGATTTTGCAACCTA TTACTGTCAACAGAGTGACAACACAAGA (SEQ ID NO: 381) 7 7 B cells A_24_P510357 S76132 Ig V lambda II = IgG rheumatoid factor [human, CATCACTGGTCTCCAGGCTGAGGACGAGGCT hybridoma AEE111F, mRNA Partial, 315 nt]. GATTATTACTGCAGCTCATATACAAGCAG (SEQ ID NO: 382) 7 9 B cells A_24_P605563 S42404 Ig lambda chain = anti-Rh(D) antibody [human, AAGATAGCAGCCCCGTCAAGCGGGAGTGGAG mRNA Partial, 642 nt]. ACCACCACACCCTCCAAACAAAGCAACAA (SEQ ID NO: 383) 7 5 B cells A_24_P608268 CCAGAGATGATTCCAAGAACACGGCGTATCTG CAAATGAACAGCCTGAAAACCGAGGACA (SEQ ID NO: 384) 7 5 B cells A_24_P626951 GACAGAGTCACCATCACTTGTCGGGCGAGTCA GGGAATTAGCAATTATTTAGCCTGGTTT (SEQ ID NO: 385) 7 3 B cells A_24_P66578 GCAGATTACACTCTCACCATCCGCAGCCTGCA GCCTGAAGATTTTGCAAATTATTACTGT (SEQ ID NO: 386) 7 6 B cells A_24_P702749 ATGCAGACTCCGTGAAGGGCCGATTCACCATC TCCAGAGACAATTCCAAGAACACGGTGT (SEQ ID NO: 387) 7 4 B cells A_24_P76868 HSZ74662 H. sapiens mRNA for immunoglobulin, light chain, TGGGCATCACCGGACTCCAGACTGGGGACGA V-J region. GGCCGATTATTACTGCGGAACATGGAATA (SEQ ID NO: 388) 7 6 B cells A_24_P83102 NM_001013618 LOC91353 Homo sapiens similar to omega protein TCCAAGCCAACAAGGCTACACTGGTGTGTCTC (LOC91353), mRNA ATGAATGACTTTTATCCGGGAATCTTGA (SEQ ID NO: 389) 7 3 B cells A_24_P852001 HSA234192 Homo sapiens mRNA for Ig heavy chain variable AGTTTGGGCTGAGCTGCCTTTTTCTTGTGGCT region, clone C2. ATTTTAAAAGGTGTCCAGTGTGAGGTGC (SEQ ID NO: 390) 7 6 B cells A_32_P148118 CAGCAGCCTGCAGCCTGAAGATTTTGCAGCTT ATTACTGTCAACAGAGTGACAGTACCCC (SEQ ID NO: 391) 7 3 B cells A_32_P157927 AC096579 Homo sapiens BAC clone RP11-601N4 from 2, GGCCACCATCAACTGCAAGTCCAGCCAGAGT complete sequence. GTTTTATACAGCTCCAAGAATAAGAACTA (SEQ ID NO: 392) 7 6 B cells A_32_P159192 AGCAGCCTGCAGCCTGAAGATTTTGCAGTTTA TTACTGTCAGCAGGATIATMCTTACCT (SEQ ID NO: 393) 7 13 B cells A_32_P200144 XM_939003 LOC649923 PREDICTED: Homo sapiens similar to Ig gamma- CGTGAGGATGCTTGGCACGTACCCCGTGTAC 2 chain C region (LOC649923), mRNA ATACTTCCCAGGCACCCAGCATGGAAATA (SEQ ID NO: 394) 7 7 B cells A_32_P39440 GTGGGTCTGGGACAGAGTTCACTCTCACCATC AGCAGCCTGCAGTCTGAAGATTTTGCAG (SEQ ID NO: 395) 7 4 B cells A_32_P43664 NM_144646 IGJ Homo sapiens immunoglobulin J polypeptide, TCTGTCATAAGTGTAGCAGGTCTCTGTAGCAC linker protein for immunoglobulin alpha and mu TGTCTTCATCACAGATATTGCTCTGGGT (SEQ polypeptides (IGJ), mRNA ID NO: 396) 7 3 B cells A_32_P722809 XM_940969 LOC651751 PREDICTED: Homo sapiens similar to Ig kappa GATTTTACACTGAAAATCAGCAGAGTGGAGGC chain V-II region RPMI 6410 precursor TGAGGATGTTGGGGTTTATTACTGCATG (SEQ (LOC651751), mRNA ID NO: 397) 8 all cell types 8 A_23_P148473 NM_000206 IL2RG Homo sapiens interleukin 2 receptor, gamma CTTTCCTGTTTGCATTGGAAGCCGTGGTTATC (severe combined immunodeficiency) (IL2RG), TCTGTTGGCTCCATGGGATTGATTATCA (SEQ mRNA ID NO: 398) 8 A_23_P21057 NM_052838 SEPT1 Homo sapiens septin 1 (SEPT1), mRNA ATTTCCTGAACCTGCGACGGATGCTGGTGCAG ACACACCTGCAGGACCTGAAAGAGGTGA (SEQ ID NO: 399) 8 A_23_P213424 NM_003633 ENC1 Homo sapiens ectodermal-neural cortex (with BTB- GTTGGAGGATACTTTGGCATTCAGCGATGCAA like domain) (ENC1), mRNA GACTTTGGACTGCTACGATCCAACATTA (SEQ ID NO: 400) 8 A_23_P25069 XM_927026 LOC440080 PREDICTED: Homo sapiens similar to cDNA TTTACTCCAACCATGTCATCCATTGAAGAGCTT sequence BC048546, transcript variant 2 GAAAACAAGGGCCAAGTGATGAAGACT (SEQ (LOC440080), mRNA ID NO: 401) 8 A_23_P26810 NM_000546 TP53 Homo sapiens tumor protein p53 (Li-Fraumeni CTGTGAGGGATGTTTGGGAGATGTMGAAATG syndrome) (TP53), mRNA TTCTTGCAGTTAAGGGTTAGTTTACAAT (SEQ ID NO: 402) 8 A_23_P301925 MIHSXX H. sapiens mitochondrial genome. CTACGTTGTAGCCCACTTCCACTATGTCCTATC AATAGGAGCTGTATTTGCCATCATAGG (SEQ ID NO: 403) 8 A_23_P315252 HUMMTCG Human mitochondrion, complete genome. CATCGCTGGGTCAATAGTACTTGCCGCAGTAC TCTTAAAACTAGGCGGCTATGGTATAAT (SEQ ID NO: 404) 8 A_23_P337726 MIHSXX H. sapiens mitochondrial genome. CATGGCCATCCCCTTATGAGCGGGCACAGTG ATTATAGGCTTTCGCTCTAAGATTAAAAA (SEQ ID NO: 405) 8 A_23_P402751 MTHSCOXII Homo sapiens mitochondrial coxII mRNA for GACTCCTTGACGTTGACAATCGAGTAGTACTC cytochrome C oxidase II subunit. CCGATTGAAGCCCCCATTCGTATAATAA (SEQ ID NO: 406) 8 A_23_P70095 NM_001025158 CD74 Homo sapiens CD74 antigen (invariant polypeptide AAGATCAGAAGCCAGTCATGGATGACCAGCG of major histocompatibility complex, class II CGACCTTATCTCCAACAATGAGCAACTGC antigen-associated) (CD74), transcript variant 3, (SEQ ID NO: 407) mRNA 8 A_23_P86943 NM_003139 SRPR Homo sapiens signal recognition particle receptor GCTAGGCTGGAGTGATTTGTTACAAATGAGCA (‘docking protein’) (SRPR), mRNA AAAGATGAGTCCTTGCTTCCCTCAGAAA (SEQ ID NO: 408) 8 A_23_P98884 NM_005785 RNF41 Homo sapiens ring finger protein 41 (RNF41), TTCCAGATGAGCTCTTCTTTCCTACAAGTTTTC transcript variant 1, mRNA ATAATTAGGGAATGCCAGGGTTTAGGG (SEQ ID NO: 409) 8 A_24_P202319 NM_005173 ATP2A3 Homo sapiens ATPase, Ca++ transporting, CAACTTCTACCAGCTGAGGAACTTCCTGAAGT ubiquitous (ATP2A3), transcript variant 1, mRNA GCTCCGAAGACAACCCGCTCTTTGCCGG (SEQ ID NO: 410) 8 A_24_P204334 CTAGCCAIGGCCATCCCCTTAAGCGGGGTGAT TATAGGCTTTCGCTCTAAGATTAAAAAT (SEQ ID NO: 411) 8 A_24_P350200 AAGGCCACCACACACCACCTGTCCAGAAAGG CCTTCGATACGGGATAATCCTATTTATTA (SEQ ID NO: 412) 8 A_24_P381224 NM_032431 SYVN1 Homo sapiens synovial apoptosis inhibitor 1, AAGTTTAGAATTGGAATTACTTCCTTACTAGTG synoviolin (SYVN1), transcript variant 1, mRNA TCTTTTGGCTTAAATTTTGTCTTTTGA (SEQ ID NO: 413) 8 A_24_P416728 NM_001130 AES Homo sapiens amino-terminal enhancer of split ACGGCTTGAACATCGAGATGCACAAACAGGCT (AES), transcript variant 2, mRNA GAGATCGTCAAAAGGCTGAACGGGATTT (SEQ ID NO: 414) 8 A_24_P551842 CTCCGATCCGTCCCTAAACAAACTAGGAGGCG TCCTTTGCCCTATTATATCCATCCTCAT (SEQ ID NO: 415) 8 A_24_P700170 NM_014225 PPP2R1A Homo sapiens protein phosphatase 2 (formerly ACGGCTGAACATCATCTCTAACCTGGACTGTG 2A), regulatory subunit A (PR 65), alpha isoform TGAACGAGGTGATTGGCATCCGGTCAGC (SEQ (PPP2R1A), mRNA ID NO: 416) 8 A_24_P710024 TTAGCATCATCCCTCTACTATTTTTTAGCCAAA TCAACAACAACCTATTTTAGCTGTTCC (SEQ ID NO: 417) 8 A_24_P713185 AATATGACTAGCTTACACAATAGCTCACATAGT ACAGATACTCTTTACGGACTCCACTTA (SEQ ID NO: 418) 8 A_24_P910169 TTACATGGGTTTTCATGATCAGCCGCGAAACT GAGAACGTCAGGTCAGCGAGGAGATTGG (SEQ ID NO: 419) 9 B cells 9 5 B cells A_23_P10356 NM_021777 ADAM28 Homo sapiens ADAM metallopeptidase domain 28 CTTAGAAGCTTCGAACTGAAAATCATGGAAAG (ADAM28), transcript variant 3, mRNA GTTTTAAGATTTGAGGTTGGTTTTAGGG (SEQ ID NO: 420) 9 9 B cells A_23_P113572 NM_001770 CD19 Homo sapiens CD19 antigen (CD19), mRNA TACATGCCAGTGACACTTCCAGTCCCCTTTGT ATTCCTTAAATAAACTCAATGAGCTCTT (SEQ ID NO: 421) 9 6 B cells A_23_P116371 NM_021950 MS4A1 Homo sapiens membrane-spanning 4-domains, GAGCTCACACACCATATATTAACATATACAACT subfamily A, member 1 (MS4A1), transcript variant GTGAACCAGCTAATCCCTCTGAGAAAA (SEQ 3, mRNA ID NO: 422) 9 6 B cells A_23_P121657 NM_005114 HS3ST1 Homo sapiens heparan sulfate (glucosamine) 3-O- GGCAGAACATTTGACTGGCACTGATTTGCAAT sulfotransferase 1 (HS3ST1), mRNA AAGCTAAGCTCAGAAACTTTCCTACTGT (SEQ ID NO: 423) 9 A_23_P125618 NM_000808 GABRA3 Homo sapiens gamma-aminobutyric acid (GABA) TGCATGCCTGCCCACTGAAGTTTGGAAGCTAT A receptor, alpha 3 (GABRA3), mRNA GCCTATACAACAGCTGAAGTGGTTTATT (SEQ ID NO: 424) 9 4 B cells A_23_P149368 NM_052938 FCRL1 Homo sapiens Fc receptor-like 1 (FCRL1), mRNA AAACAAGATGGAATAAAAGAAATTGGGATCTT GGGTTGGAGGGACAGTGAAGCTTAGAGC (SEQ ID NO: 425) 9 A_23_P151166 NM_032369 MGC15619 Homo sapiens hypothetical protein MGC15619 TCTAGAAAAGTCTCTTATTTTCAAGCTGTTCTA (MGC15619), mRNA AATAGCTTCGTCTCAGTTTCCCCAAAA (SEQ ID NO: 426) 9 9 B cells A_23_P160751 NM_030764 FCRL2 Homo sapiens Fc receptor-like 2 (FCRL2), GAGGAATCAGAAGGGAAGATCAACAGCAAGG transcript variant 2, mRNA ATGGGGCATCATTAAGACTTGCTATAAAA (SEQ ID NO: 427) 9 4 B cells A_23_P207201 NM_000626 CD79B Homo sapiens CD79B antigen (immunoglobulin- CGCTGAAGGATGGTATCATCATGATCCAGACG associated beta) (CD79B), transcript variant 1, CTGCTGATCATCCTCTTCATCATCGTGC (SEQ mRNA ID NO: 428) 9 7 B cells A_23_P209055 NM_001771 CD22 Homo sapiens CD22 antigen (CD22), mRNA GCCTCAGGCACAAGAAAATGTGGACTATGTGA TCCTCAAACATTGACACTGGATGGGCTG (SEQ ID NO: 429) 9 4 B cells A_23_P250245 NM_001782 CD72 Homo sapiens CD72 antigen (CD72), mRNA TGCTCAAAGCTCAAAATGTAACAAGGTACATAA AACTTGGTCATGGTGGACACTGGAGTC (SEQ ID NO: 430) 9 A_23_P307382 NM_080552 SLC32A1 Homo sapiens solute carrier family 32 (GABA CCAGCTTGCCTGCCGGTTTTCAGGAATCTAAA vesicular transporter), member 1 (SLC32A1), CTCTCATCTTGTGCAATTTATCAGGTGT (SEQ mRNA ID NO: 431) 9 5 B cells A_23_P31725 NM_001715 BLK Homo sapiens B lymphoid tyrosine kinase (BLK), TCGCACGGTCATCCGGAGTACTAAGCCCCAGT mRNA AAGGTGTTCAGGACTGGTAAGCGACTGT (SEQ ID NO: 432) 9 5 B cells A_23_P357717 NM_021966 TCL1A Homo sapiens T-cell leukemia/lymphoma 1A TTTCCCCCCTTTATAGATGGTCACGCACCTGG (TCL1A), mRNA GTGTTACAAAGTTGTATGTGGCATGAAT (SEQ ID NO: 433) 9 A_23_P398294 NM_003959 HIP1R Homo sapiens huntingtin interacting protein 1 GTTAGCATTTCCTCCTGAAGTGTTCTGTTGGC related (HIP1R), mRNA AATAAAATGCACTTTGACTGTTTGTTGT (SEQ ID NO: 434) 9 A_23_P76402 NM_024549 FLJ21127 Homo sapiens tectonic (FLJ21127), mRNA GCTTTGGTTATAGAAGTGAAGTGGACTAAATA CGGATCCCTGCTGAATCCACAGGCCAAA (SEQ ID NO: 435) 9 2 B cells A_23_P904 NM_024603 C1orf165 Homo sapiens chromosome 1 open reading frame CATCGTCAGAGAGTGTTTGTATGACAGAATAG 165 (C1orf165), mRNA CACAAGAAACTGTGGATGAAACTGAAAT (SEQ ID NO: 436) 9 4 B cells A_24_P203056 NM_001024808 BCL7A Homo sapiens B-cell CLL/lymphoma 7A (BCL7A), TCGCCAAGAACCTGGTTAGAGGCATAAAGACC transcript variant 2, mRNA TTTTTTCACCGTTACCTAATTTTTTCCC (SEQ ID NO: 437) 9 4 B cells A_24_P252945 NM_001716 BLR1 Homo sapiens Burkitt lymphoma receptor 1, GTP TTTTCTTTTTAATAAAAAGGCACCTATAAAACA binding protein (chemokine (C-X-C motif) receptor GGTCAATACAGTACAGGCAGCACAGAG (SEQ 5) (BLR1), transcript variant 1, mRNA ID NO: 438) 9 A_24_P254106 AACACTATTGTAGGTAGTGATATGTGTGTTAG GAAAAAAATAAGGCCGAGAGAGGGGAGT (SEQ ID NO: 439) 9 A_24_P305067 NM_024015 HOXB4 Homo sapiens Homo box B4 (HOXB4), mRNA GATCAACTCAAACTATGTCGACCCCAAGTTCC CTCCATGCGAGGAATATTCACAGAGCGA (SEQ ID NO: 440) 9 3 B cells A_24_P324838 HSIGCMUDE Human immunoglobulin C(mu) and C(delta) heavy AGATGGTGCAGTGGTTAGAGCTGAGGCTTATC chain genes (constant regions). CCACAGAGAACCCTGGCGCCTTGGTCAA (SEQ ID NO: 441) 9 4 B cells A_24_P413126 NM_020182 TMEPAI Homo sapiens transmembrane, prostate androgen AAGAAACTGCTTGTTGTGTATCAGTAATCATTA induced RNA (TMEPAI), transcript variant 1, GTGGCAATGATGACATTCTGAAAAGCT (SEQ mRNA ID NO: 442) 9 8 B cells A_24_P417352 HSIGCMUS Human C mu gene for IgM heavy chain exons CH1 TGACCACCTATGACAGCGTGACCATCTCCTGG 4, secretory. ACCCGCCAGAATGGCGAAGCTGTGAAAA (SEQ ID NO: 443) 9 8 B cells A_24_P621701 HS250D10 Human DNA sequence from clone CTA-250D10 TGGTAAGTTTCTCTCTCTTTAGAGACTCCACAA on chromosome 22 TAAAGTTTTCAACATGGTAAGGTTTTC (SEQ ID NO: 444) 9 7 B cells A_24_P64344 NM_013314 BLNK Homo sapiens B-cell linker (BLNK), mRNA TAAGCGAGTATATAATATTCCTGTGCGATTTAT TGAAGCAACAAAACAATATGCCTTGGG (SEQ ID NO: 445) 9 A_24_P916364 AC007172 Homo sapiens chromosome 9, clone GGGTGAATGTTTGAAAATCATGAATCAGCCAC hRPK.538_E_7, complete sequence. CATTATTAATTGAAGAGCTGGGAATACC (SEQ ID NO: 446) 9 7 B cells A_24_P940348 NM_173544 BCNP1 Homo sapiens B-cell novel protein 1 (BCNP1), AGACAAGCTTTTACCGACTTCCTCTGCTTGCC mRNA AGCAAAGTCATCTGCTAACTGGATATTG (SEQ ID NO: 447) 9 A_24_P95723 NM_014792 KIAA0125 Homo sapiens KIAA0125 (KIAA0125), mRNA CCATTTTAAAGATGGCTACTTAGGACCATATG GATGTTGTACTGATGTCATTTGACCACG (SEQ ID NO: 448) 9 A_32_P107002 NM_001012391 LOC400509 Homo sapiens similar to FLJ12363 protein TGTGAAAAGCATCGATGATGAAGATGTGGATG (LOC400509), mRNA AAAACGAAGATGACGTGTATGGAAACTC (SEQ ID NO: 449) 9 3 B cells A_32_P13337 AC006230 Homo sapiens chromosome 4 clone C0287J14 ATCCTCCATGGTATCTGAATCCCAGAATCCTA map 4p16, complete sequence. CAATCCTGCATGGTATCTGAAACATACT (SEQ ID NO: 450) 9 3 B cells A_32_P137819 AL450344 Human DNA sequence from clone RP11-136K14 CTGCAGATCTTTATTACTGGCAAGAAAGTCCC on chromosome 6 Contains three novel genes, the AGAAGTTCTTTTCTCTAACTTATGACTA (SEQ 5′ end of a novel gene (contains FLJ31738 and ID NO: 451) KIAA1209) and a CpG island, complete sequence. 9 4 B cells A_32_P356316 NM_002119 HLA-DOA Homo sapiens major histocompatibility complex, TGGAAAGGTGTTTCTCTCATCTCTGTCCTAAG class II, DO alpha (HLA-DOA), mRNA GCTTGATAAAGTCATTAAAATTGTGTTC (SEQ ID NO: 452) 9 3 B cells A_32_P57013 NM_018014 BCL11A Homo sapiens B-cell CLL/lymphoma 11A (zinc ATAATACAAAGATGGCGCAGGGAAGATGAATT finger protein) (BCL11A), transcript variant 2, GTGGGAGAGCCGTCATGGCTTTTTTTTA (SEQ mRNA ID NO: 453) 9 A_32_P64016 CTCTGAGGCTAAGATTACTGGTGTACTCATTG GGACCAGTTTGGTCTCAGTGACTGAAAA (SEQ ID NO: 454) 9 9 B cells A_32_P71876 AL356276 Human DNA sequence from clone RP11-367J7 on GAAGTTTGAACTTCTTTGTATTGTATGATCATC chromosome 1 CCTTTACCTTAATACTCACATGAAATG (SEQ ID NO: 455) 9 A_32_P8813 GACGGGACATCATGCTGGGCAACACAGCTAA AATGCGGGTGAAGACCAGATTTCTTGCAC (SEQ ID NO: 456) 10 all cell types 10 A_23_P117480 CNS06C82 Human chromosome 14 DNA sequence BAC C- ATTGTCGGCATCTTCCATGCTCTGAGTCAGTT 2335L22 of library CalTech-D from chromosome AGCATTTACAGTGAATCTGCCCTTCTGT (SEQ 14 of Homo sapiens (Human), complete ID NO: 457) sequence. 10 A_23_P153827 NM_005934 MLLT1 Homo sapiens myeloid/lymphoid or mixed-lineage TACACCGGAGGCTGATGGCGCTGCGGGAGCG leukemia (trithorax Homolog, Drosophila); CAACGTGCTGCAGCAGATTGTGAATCTGA translocated to, 1 (MLLT1), mRNA (SEQ ID NO: 458) 10 A_23_P170464 NM_031297 DKFZP761H1 Homo sapiens hypothetical protein TGGCCCCAGAGGATGAGGTCATTGTGAATCAG 710 DKFZp761H1710 (DKFZP761H1710), mRNA TACGTGATTCGGCCTGGCCCCTCGGCCT (SEQ ID NO: 459) 10 A_23_P258887 NM_012190 ALDH1L1 Homo sapiens aldehyde dehydrogenase 1 family, TTCGGGCCTGTCATGATCATCTCTGGGTTTGC member L1 (ALDH1L1), mRNA TGATGGGGACTTGGATGCCGTGCTGTCT (SEQ ID NO: 460) 10 A_23_P30805 NM_003541 HIST1H4K Homo sapiens histone 1, H4k (HIST1H4K), mRNA AAGCGCCAGGGCCGCACCCTCTACGGTTTCG GTGGTTGAGCGTCCCTTTCTATCAATAAA (SEQ ID NO: 461) 10 A_23_P390504 NM_001453 FOXC1 Homo sapiens forkhead box C1 (FOXC1), mRNA CCTTCCAGCCAGTCTCTGTACCGCACGTCCGG AGCTTTCGTCTACGACTGTAGCAAGTTT (SEQ ID NO: 462) 10 A_23_P407695 NM_147161 ACOT11 Homo sapiens acyl-CoA thioesterase 11 AGCGGACCTCAGGGCGGAGGCTTCCCACGG (ACOT11), transcript variant 2, mRNA GGAGGCAGGAAGAAATAAAGGTCTTTGGCT (SEQ ID NO: 463) 10 A_23_P432506 NM_152757 FLJ30313 Homo sapiens hypothetical protein FLJ30313 GTGGGGAGGGTTTCTTGGGTTTCTTGAAGCCA (FLJ30313), mRNA GTATTTCCCATAGTATCTTACGTCCCAG (SEQ ID NO: 464) 10 A_23_P46894 NM_020549 CHAT Homo sapiens choline acetyltransferase (CHAT), TAGCCTCCTCGGCAGAAAAACTTCAACGAATA transcript variant M, mRNA GTAAAGAACCTTGACTTCATTGTCTATA (SEQ ID NO: 465) 10 A_23_P57089 NM_020182 TMEPAI Homo sapiens transmembrane, prostate androgen GCCGGGCTGGGGCTGCGTAGGTGAAAAGGCA induced RNA (TMEPAI), transcript variant 1, GAACACTCCGCGCTTCTTAGAAGAGGAGT mRNA (SEQ ID NO: 466) 10 A_23_P69652 NM_080819 GPR78 Homo sapiens G protein-coupled receptor 78 GCTCGTGCCCTTCGTCACCGTGAACGCCCAG (GPR78), mRNA TGGGGCATCCTCAGCAAGTGCCTGACCTA (SEQ ID NO: 467) 10 A_23_P75283 NM_006744 RBP4 Homo sapiens retinol binding protein 4, plasma TCAGTTCCCATAAAACCTTCATTACACATAAAG (RBP4), mRNA ATACACGTGGGGGTCAGTGAATCTGCT (SEQ ID NO: 468) 10 A_23_P93217 NM_006672 SLC22A7 Homo sapiens solute carrier family 22 (organic AGTGAACTTCTCCTATTACGGCCTGAGTCTGG anion transporter), member 7 (SLC22A7), ATGTGTCGGGGCTGGGGCTGAACGTGTA transcript variant 1, mRNA (SEQ ID NO: 469) 10 A_24_P187539 ACGAATATGCGTTCGACAAGCCGGTCCCGAAA GACATGGTCATCTGGAATCGTGAACGGG (SEQ ID NO: 470) 10 A_24_P297539 NM_007019 UBE2C Homo sapiens ubiquitin-conjugating enzyme E2C TTGTCTTTTAAATTAAGCCTCGGTTGAGCCCTT (UBE2C), transcript variant 1, mRNA GTATATTAAATAAATGCATTTTTGTCC (SEQ ID NO: 471) 10 A_24_P302172 NM_000959 PTGFR Homo sapiens prostaglandin F receptor (FP) CCCATTCAAATTGTCCTAGGTCTATCAGAAATT (PTGFR), mRNA AGGGAAGGTAGTCCTGCTTTATAATAG (SEQ ID NO: 472) 10 A_24_P322229 NM_033315 RASL10B Homo sapiens RAS-like, family 10, member B TGGGGGAAGGGTCGTGGGTGGGGAATTTATC (RASL10B), mRNA ACCAACATCCATTGTAGGGGGAATCTATG (SEQ ID NO: 473) 10 A_24_P396489 HSM807143 Homo sapiens mRNA; cDNA DKFZp686E15252 AGCTTTGCTTTGCAAAGATTGATGACAGACTG (from clone DKFZp686E15252). GTTCCTCAGAGGCCTAGGCTACCCGTCA (SEQ ID NO: 474) 10 A_24_P418176 NM_001007238 HRES1 Homo sapiens HTLV-1 related endogenous GCGGGCTGGGCGCTCTGGCGGTGTGCGCTG sequence (HRES1), mRNA AGGTGGGCAGAGCGGCAGGTGGGGGCGTTG (SEQ ID NO: 475) 10 A_24_P636974 NM_001013665 LOC399744 Homo sapiens hypothetical LOC399744 GTGGGAGGGGCCGGTGTGAGGCAAGGCTCA (LOC399744), mRNA CGCTGACCTCTCTCGGCGTGGGAGGGGCCG (SEQ ID NO: 476) 10 A_24_P741378 AC027682 Homo sapiens chromosome 16 clone CTD- CACAGAAACATACAAGGAAGGCACCCCCGCTC 2012K14, cemplete sequence. TGTGGGCGAGACAAAGCAGCAATCCTCT (SEQ ID NO: 477) 10 A_24_P810084 AC016394 Homo sapiens chromosome 10 clone RP11- GGAATTGGCTCTTCCTATTTCCCTACTTCATGA 152N13, complete sequence. AAACTCCAGTAGAAGACCTTAGAACCT (SEQ ID NO: 478) 10 A_24_P8298 AC026740 Homo sapiens chromosome 5 clone CTD- TTTAAACACACGTGGTCCCCCGTCTAGAAGCC 2589H19, complete sequence. TCTGCATTTAAGCACACGTGGTCCCCCG (SEQ ID NO: 479) 10 A_32_P138032 NM_006365 C1orf61 Homo sapiens chromosome 1 open reading frame ATGGCTAAGTTGGGAGACCAAAAAGAAGAATG 61 (C1orf61), mRNA TACTTCATCTGGTTGGGCTGGATTCCCT (SEQ ID NO: 480) 10 A_32_P187571 NM_004588 SCN2B Homo sapiens sodium channel, voltage-gated, TGTGACTCGACTGCTGGGATGTATCTGCTTTT type II, beta (SCN2B), mRNA GGGAGCAGACTGAGTTTCTTTTGCAATT (SEQ ID NO: 481) 10 A_32_P219148 NM_001013725 LOC441268 Homo sapiens hypothetical gene supported by TCCCCGTCCACGTTACCGCATTCAGAGCTTGG BC044942 (LOC441268), mRNA GTCACCTGGACACTGAACTCAGGTGAAT (SEQ ID NO: 482) 10 A_32_P222149 XM_499058 LOC442512 PREDICTED: Homo sapiens similar to U2 small TACAGAGCAGTCGCCGGGCAGTTGAAGATCA nuclear ribenucleoprotein A (U2 snRNP-A) GCTAAAGATATGTGGCCACAGGAGGGATG (LOC442512), mRNA (SEQ ID NO: 483) 10 A_32_P52386 AC004080 Homo sapiens PAC clone RP1-170O19 from 7p15-p21, AAATGTGGCGCTCTCGCCAAGAAAAAGCTTGG complete sequence. GGACTGAATTCTTGAGATTTATGGTGCA (SEQ ID NO: 484) 10 A_32_P71710 NM_000577 IL1RN Homo sapiens interleukin 1 receptor antagonist AAGATTTTATTGTAAAACAGAGCTGAAGTCACA (IL1RN), transcript variant 3, mRNA GGAAGTAGGGAACTTTGCACCCAACAT (SEQ ID NO: 485) 11 all cell types 11 A_23_P128974 NM_006399 BATF Homo sapiens basic leucine zipper transcription TATTAAGAAAGATGCTCAAGTCCCATGGCACA factor, ATF-like (BATF), mRNA GAGCAAGGCGGGCAGGGAACGGTTATTT (SEQ ID NO: 486) 11 A_23_P218731 NM_005111 CRYZL1 Homo sapiens crystallin, zeta (quinone AAGATGATGAACCAGCTGTAAAACTACAACTA reductase)-like 1 (CRYZL1), transcript CTACCACATAAACATGATATCATCACAC (SEQ variant 1, mRNA ID NO: 487) 11 A_23_P42514 NM_030939 C6orf62 Homo sapiens chromosome 6 open reading frame TCCTTTGGAGTAAAACTAGTGCTTACCAGTTTC 62 (C6orf62), mRNA CAATTGTATTTAGCTTCTGGTTGGAAT (SEQ ID NO: 488) 11 A_23_P92967 NM_004531 MOCS2 Homo sapiens molybdenum cofactor synthesis 2 AAGCATATCTACCCATGGCGGAAAATGAAGTC (MOCS2), transcript variant 3, mRNA AGAAAGATTTGTAGTGACATTAGGCAGA (SEQ ID NO: 489) 11 A_32_P160615 AC016554 Homo sapiens chromosome 5 clone CTC-340H12, ACTGCAATGAACACATATACATATACATCCAAA complete sequence. CATTCCTCCATTCGTCTATTAATCTGC (SEQ ID NO: 490) 11 A_32_P37461 CATCAACTGGTAAACAAAAAACTGTGAGAACG GATCCTGAATCTTGCGCTTACCAGGGGA (SEQ ID NO: 491) 12 all cell types 12 A_23_P100711 NM_000304 PMP22 Homo sapiens peripheral myelin protein 22 TGTGCCTCCAAGGACTGTCTGGCAATGACTTG (PMP22), transcript variant 1, mRNA TATTGGCCACCAACTGTAGATGTATATA (SEQ ID NO: 492) 12 A_23_P135730 NM_145295 ZNF627 Homo sapiens zinc finger protein 627 (ZNF627), ACTCCCCTAGTCTGTAGACGGAATTGGCATAC mRNA GGTCTAATTTGTGTAGTAAGCACCTTTG (SEQ ID NO: 493) 12 A_23_P307968 NM_022124 CDH23 Homo sapiens cadherin-like 23 (CDH23), CCATCTGACGCTACAGTCACCACGACCTTCAA transcript variant 1, mRNA TATCCTGGTTATTGACATCAATGACAAT (SEQ ID NO: 494) 12 A_23_P411162 NM_003894 PER2 Homo sapiens period Homolog 2 (Drosophila) TCCTCCTGAAAAGAGAATTTTTACAACCACCCA (PER2), transcript variant 2, mRNA TACACCAAATTGTTTGTTCCAGGATGT (SEQ ID NO: 495) 12 A_23_P63343 NM_006786 UTS2 Homo sapiens urotensin 2 (UTS2), transcript AGAATCTGGAAACCATACAAGAAACGTGAGAC variant 2, mRNA TCCTGATTGCTTCTGGAAATACTGTGTC (SEQ ID NO: 496) 12 A_23_P64879 NM_004982 KCNJ8 Homo sapiens potassium inwardly-rectifying CTTCCCTCATGGTACCAAAGGTGCAATTTATG channel, subfamily J, member 8 (KCNJ8), mRNA ACTCCAGAAGGAAATCAAAACACATCGG (SEQ ID NO: 497) 12 A_24_P45620 NM_006786 UTS2 Homo sapiens urotensin 2 (UTS2), transcript AGAAAGTTTCAGGATTTCTCTGGACAAGATCC variant 2, mRNA TAACATTTTACTGAGTCATCTTTTGGCC (SEQ ID NO: 498) 12 A_24_P614702 AC091320 Homo sapiens BAC clone RP11-447A2 from 7, CCTTCCTCATTTTGGAACTTAAGGTTGTGTACA complete sequence GAACAGTCTTACAATGACAGTGTTTAG (SEQ ID NO: 499) 12 A_32_P31144 TTCTATACCTCTAAGCTGTTCTTTTCTGAACCA TGAATCGGGAGAATTATTGTCACTCAT (SEQ ID NO: 500) 12 A_32_P427222 XM_291007 LOC339766 PREDICTED: Homo sapiens hypothetical protein TCTCTACCGCTTCTTGCTAGAAACAATGGCCT LOC339766 (LOC339766), mRNA ATGTTAAAAATAACTTGTCAAGAATCAG (SEQ ID NO: 501) 13 Red Blood cells 13 A_23_P109322 NM_006198 PCP4 Homo sapiens Purkinje cell protein 4 (PCP4), CCCTCCTAGTCCACCTGAAAACACCAAATTCA mRNA ACCATCATCTGTCAAGAAATTAAAAGAA (SEQ ID NO: 502) 13 3 RBC A_23_P11408 NM_001002758 PRY2 Homo sapiens PTPN13-like, Y-linked 2 (PRY2), ACCTCCTTCTCTTCTGGACATGTCCAGGAGTG mRNA GCCGTTGCTACAAGTCACCTGGTGCTAC (SEQ ID NO: 503) 13 A_23_P135568 AC026315 Homo sapiens 3 BAC RP11-114D6 (Roswell Park AGCAAGATATCCTCCTCATGGTCCCTTTAGCT Cancer Institute Human BAC Library) complete CTCAAAAGCAATGAAATCCTCCTGTTCT (SEQ sequence. ID NO: 504) 13 A_23_P161474 NM_018518 MCM10 Homo sapiens MCM10 minichromosome CCTCCTGTGACTCTGGAAAGCAAAGGATTGGC maintenance deficient 10 (S. cerevisiae) (MCM10), TGTGTATTGTCCATTGATTCCTGATTGA (SEQ transcript variant 2, mRNA ID NO: 505) 13 A_23_P204998 NM_005766 FARP1 Homo sapiens FERM, RhoGEF (ARHGEF) and TCCTCCTGCAACTGTGGTTTGAAACTGCGCAT pleckstrin domain protein 1 (chondrocyte-derived) TCTCTAGTAGTATATATCGTGCCTGTCT (SEQ (FARP1), transcript variant 1, mRNA ID NO: 506) 13 3 RBC A_23_P205637 NM_015163 TRIM9 Homo sapiens tripartite motif-containing 9 CCTCCTCGACTTAAATAGAAAAAACTTGACATT (TRIM9), transcript variant 1, mRNA TTTTATCAACGATGAACAACAAGGTCC (SEQ ID NO: 507) 13 A_23_P215549 NM_000940 PON3 Homo sapiens paraoxonase 3 (PON3), mRNA GCACCTCTGTGGCTTCTGTGTACCATGGGAAA ATTCTCATAGGCACCGTATTTCACAAAA (SEQ ID NO: 508) 13 A_23_P254626 NM_003919 SGCE Homo sapiens sarcoglycan, epsilon (SGCE), ACTGGTCCTTTTTCTAATACTTGCTTATATCAT mRNA GTGCTGCCGACGGGAAGGCGTGGAAAA (SEQ ID NO: 509) 13 A_23_P26582 NM_020988 GNAO1 Homo sapiens guanine nucleotide binding protein TTGTACTGACCTCTTGTCCTGTATAGCAACCTA (G protein), alpha activating activity TTTGACTGCTTCACGGACTCTTTGCTG (SEQ ID polypeptide O (GNAO1), transcript variant 1, mRNA NO: 510) 13 A_23_P303803 NM_152474 C19orf18 Homo sapiens chromosome 19 open reading CAGCTCGAGTCACTTTATAAGAACCTCAGGAT frame 18 (C19orf18), mRNA ACCGTTATTAGGAGATGAAGAAGAGGGC (SEQ ID NO: 511) 13 A_23_P309278 NM_173158 NR4A1 Homo sapiens nuclear receptor subfamily 4, group CTCCCTTGCCACCCAAATGTTAGAAAAATAGCT A, member 1 (NR4A1), transcript variant 3, mRNA GTGAACAGAGAGCGCTTTTGTCTGCAA (SEQ ID NO: 512) 13 A_23_P326844 NM_174913 C14orf21 Homo sapiens chromosome 14 open reading ACTCCTGGTCTTGTACTTCGAAGTCTGGGTGC frame 21 (C14orf21), mRNA CTTGACGGGACCACAGCTTCTGTCCCTT (SEQ ID NO: 513) 13 A_23_P44648 NM_030955 ADAMTS12 Homo sapiens ADAM metallopeptidase with CAGACCTCCAGAATTCAAAAAATGCAACCAGC thrombospondin type 1 motif, 12 (ADAMTS12), AGGCCTGCAAGAAAAGTGCCGATTTACT (SEQ mRNA ID NO: 514) 13 A_23_P68234 NM_006794 GPR75 Homo sapiens G protein-coupled receptor 75 ATCCTCCCATCATGAAACAAACTCTGCCTACAT (GPR75), mRNA GTTATCTCCAAAGCCACAGAAGAAATT (SEQ ID NO: 515) 13 A_23_P78795 NM_001009813 MEIS3 Homo sapiens Meis1, myeloid ecotropic viral CCTCCCAGACCAGAATAATATGTGGATTCGAG integration site 1 homolog 3 (mouse) (MEIS3), ACCATGAGGATAGTGGGTCTGTACATTT (SEQ transcript variant 2, mRNA ID NO: 516) 13 A_23_P80122 NM_004627 WRB Homo sapiens tryptophan rich basic protein CCTGGTAGCCTTTCCTACTAGAGTAGCAGGTG (WRB), mRNA GTGTTGGAATTACCTGTTGGATTTTAGT (SEQ ID NO: 517) 13 A_24_P126587 NM_181489 ZNF445 Homo sapiens zinc finger protein 445 (ZNF445), GCTCCTACAGGAGATGACCTCCAGAGTAAAAC mRNA AAACAAATTCATCTTAAATCAGGAACCT (SEQ ID NO: 518) 13 A_24_P136299 AC103975 Homo sapiens chromosome 15, clone RP11- TCAATTGCTTCCTCCTCAATCTGGCAGCCACT 1001M11, complete sequence. GACCTGCAGTTTGTGCTAACGCTGCCCT (SEQ ID NO: 519) 13 A_24_P200250 HSU37055 Human hepatocyte growth factor-like protein gene, CCTTCCATTAGCAACTACTCTGTACCACCCTTC complete cds. CCAAGAGTATGTCTGGAGGACTAGTGT (SEQ ID NO: 520) 13 A_24_P312594 AL133215 Human DNA sequence from clone RP11-108L7 on TTCTTCCCTCCATACATTTGCTTCCAAGTGAAT chromosome 10 TTGCATAAGCAGTGCTCAGACTGCACC (SEQ ID NO: 521) 13 A_24_P31875 NM_152577 ZNF645 Homo sapiens zinc finger protein 645 (ZNF645), CTCCTTCAACCCTACATGGTCGATCACATCATT mRNA CACACCAGAGAAGACATAGACGGTATT (SEQ ID NO: 522) 13 2 RBC A_24_P341116 NM_207378 SERPINA13 Homo sapiens serpin peptidase inhibitor, clade A CTTCCTGGTGATGACTTTCCACACGGAAACAG (alpha-1 antiproteinase, antitrypsin), member 13 GAAGCATGCTTTTTCTGGAGAAGATTGT (SEQ (SERPINA13), mRNA ID NO: 523) 13 A_24_P365349 AC008440 Homo sapiens chromosome 19 clone CTC- CCTGGCTCTGTTATTTACCGTGTATCATATGTA 331H23, complete sequence. AATATCGACAGAAACTTCAATAAACTT (SEQ ID NO: 524) 13 A_24_P409451 NM_018651 ZNF167 Homo sapiens zinc finger protein 167 (ZNF167), AAGAACTATCCTCCTGTCTGCGAAATCTTCCG transcript variant 1, mRNA GCTACACTTCAGGCAATTGTGTTACCAC (SEQ ID NO: 525) 13 4 RBC A_24_P59735 BC041372 Homo sapiens similar to seven in absentia 2, TCCTGGTTTTTGAGACTCAACCACTTTGAAAGC mRNA (cDNA clone IMAGE: 5273845), partial cds. ATTTGTGTAGCATCACAGGTGCTCCAG (SEQ ID NO: 526) 13 A_24_P607751 HSU91328 Human hereditary haemochromatosis region, CCTTCTTGGGTCAGTTAGGCCATTGGTTTCTTT histone 2A-like protein gene, hereditary TTAAAGGTTTTCAAATTTATTTGCATC (SEQ ID haemochromatosis (HLA-H) gene, RoRet gene, NO: 527) and sodium phosphate transporter (NPT3) gene, complete cds. 13 A_24_P666035 AC055716 Homo sapiens 12 BAC RP11-641A6 (Roswell Park AGTTGTACTGTCAAGGGGCAGCATTTCTGGTA Cancer Institute Human BAC Library) complete TTTCTATAATAAATTTTTCTGTGATCTC (SEQ ID sequence. NO: 528) 13 A_24_P915376 NM_006757 TNNT3 Homo sapiens troponin T type 3 (skeletal, fast) AGAAACCGAGACCCAAACTCACTGCTCCTAAG (TNNT3), mRNA ATCCCAGAAGGGGAGAAAGTGGACTTCG (SEQ ID NO: 529) 13 A_24_P920555 NM_198486 RPL7L1 Homo sapiens ribosomal protein L7-like 1 GGCATTCACTGATCCCAGCAGGTCTCCATCTA (RPL7L1), mRNA TTTGTACCAGCCTCCTCTATTCCTCCCA (SEQ ID NO: 530) 13 A_24_P927404 AC084033 Homo sapiens 12q BAC RP11-58A17 (Roswell GCCCTTTTTTGTCACTCACTGTTGTGACAGATC Park Cancer Institute Human BAC Library) CTCCGATTTCTTACATAAGTTATGCAG (SEQ ID complete sequence. NO: 531) 13 A_32_P114483 NM_153344 C6orf141 Homo sapiens chromosome 6 open reading frame GAGCCCAACTACCCTTCTGTCTTTCAACGAGA 141 (C6orf141), mRNA AAAGCGAATTTCTGGCAGGCGTGTAGCC (SEQ ID NO: 532) 13 3 RBC A_32_P133106 AP005433 Homo sapiens genomic DNA, chromosome 18 CTAATGGACTAGATTGCTGACCTTTTAATACCT clone: RP11-945C19, complete sequence. TTGGTTTTCATTGAACATACAATCACC (SEQ ID NO: 533) 13 A_32_P181638 NM_007073 BVES Homo sapiens blood vessel epicardial substance AATCCTGGTTTCCTAACCTCCTCTTGTAGTAAT (BVES), transcript variant A, mRNA TCTCAACTCAACTCAAAGTCCCAAGAA (SEQ ID NO: 534) 13 A_32_P354945 AC011503 Homo sapiens chromosome 19 clone CTB-92J24, CCCTCCTGATGATGAAGGACCTGTCATTGGAG complete sequence. AATCGACCAAAACTGACAGTGATAACTT (SEQ ID NO: 535) 13 2 RBC A_32_P5057 AC010798 Homo sapiens , clone RP11-470B24, complete CCCTGAACCTACATAGACATTTTATATCAGCAT sequence. ACAGAAAAGTAAAATCCTCCTTCAGTC (SEQ ID NO: 536) 13 A_32_P51005 BX629352 Human DNA sequence from clone WI2-80267E6 ATTCCTTTCTGGTCTCCATCCTGTCTGTAGATA on chromosome 9, complete sequence. TGTAGATCTCTTTGAAACGAAGTAAGC (SEQ ID NO: 537) 13 A_32_P524904 GGCTGAGCACTCTGTGCTGAAAACCTTTGAAC CTCACGGTGTCCTGATGAAGGAAGCAGA (SEQ ID NO: 538) 14 Red Blood cells 14 A_23_P153351 NM_000713 BLVRB Homo sapiens biliverdin reductase B (flavin CAAGGTGCCCCCACGACTGCAGGCTGTGACT reductase (NADPH)) (BLVRB), mRNA GATGACCACATCCGGATGCACAAGGTGCT (SEQ ID NO: 539) 14 7 RRC A_23_P207842 NM_000964 RARA Homo sapiens retinoic acid receptor, alpha AGTTCTCCTCCTCAGCCTTTTCCTCCTCAGTTT (RARA), transcript variant 1, mRNA TCTCTTTAAAACTGTGAAGTACTAACT (SEQ ID NO: 540) 14 3 RBC A_23_P210465 NM_002638 PI3 Homo sapiens peptidase inhibitor 3, skin-derived TCCTGCCCCATTATCTTGATCCGGTGCGCCAT (SKALP) (PI3), mRNA GTTGAATCCCCCTAACCGGTGCTTGAAA (SEQ ID NO: 541) 14 2 RBC A_23_P23850 NM_021080 DAB1 Homo sapiens disabled homolog 1 (Drosophila) CTCCCTCACCTGTACCTCAGAGGCCTTCTCCA (DAB1), mRNA GTTACTTCAACAAAGTCGGGGTGGCACA (SEQ ID NO: 542) 14 A_23_P251898 NM_152743 C7orf27 Homo sapiens chromosome 7 open reading frame GGCGCAGAAGTCTTGTGACCTCCTTCTCTTCC 27 (C7orf27), mRNA TGAGGGACAAGATTGCTTCCTACAGCAG (SEQ ID NO: 543) 14 6 RBC A_23_P332392 NM_152479 TTC9B Homo sapiens tetratricopeptide repeat domain 9B ACCTCCCCTGCAGACACCAATGTGCTCCGCTA (TTC9B), mRNA CATCCAGCTGACTCAGCTGAAGATGAAT (SEQ ID NO: 544) 14 2 RBC A_23_P338168 NM_019085 FBXL19 Homo sapiens F-box and leucine-rich repeat TCCTTCCCCCTGACCCTGACTCCTTGAACGTC protein 19 (FBXL19), mRNA ACTGAAAACGGCAGCTATTGCAAGGAGT (SEQ ID NO: 545) 14 A_23_P362893 NM_021961 TEAD1 Homo sapiens TEA domain family member 1 TTTTTTCTCCTTCCCCTTTCTTTAAGAGAGGCT (SV40 transcriptional enhancer factor) (TEAD1), GACAGATCTAGGTGTCAATCAATTGGA (SEQ mRNA ID NO: 546) 14 5 RBC A_23_P377717 NM_0112516 NOVA2 Homo sapiens neuro-oncological ventral antigen 2 CCTCCCCTTCTGGTAGTCATAGGCAGGATTGA (NOVA2), mRNA GTGACGGTTGGGAAGGGGGCTCAGAAGC (SEQ ID NO: 547) 14 A_23_P39265 NM_014400 LYPD3 Homo sapiens LY6/PLAUR domain containing 3 TCCCCTACTCCCCGCATCTTTGGGGAATCGGT (LYPD3), mRNA TCCCCATATGTCTTCCTTACTAGACTGT (SEQ ID NO: 548) 14 5 RBC A_23_P62361 NM_014235 UBL4A Homo sapiens ubiquitin-like 4A (UBL4A), mRNA GCTTCCTGCACCCTGAAGTGACTGAGACAATG GAGAAGGGGTTCTCCAAATAGAATTCTC (SEQ ID NO: 549) 14 3 RBC A_23_P67332 NM_007121 NR1H2 Homo sapiens nuclear receptor subfamily 1, group ACCACCCTCCAGCAGATAGACGCCGGCACCC H, member 2 (NR1H2), mRNA CTTCCTCTTCCTAGGGTGGAAGGGGCCCT (SEQ ID NO: 550) 14 4 RBC A_23_P79323 NM_003936 CDK5R2 Homo sapiens cyclin-dependent kinase 5, TCCCTTCAGCCCATTCCCCCTCGGTTTTATCC regulatory subunit 2 (p39) (CDK5R2), mRNA ATTTCCTTGCCTCCTTTTTGTGTCTTCA (SEQ ID NO: 551) 14 A_23_P81717 NM_024919 FRMD1 Homo sapiens FERM domain containing 1 AGGTTCCTCCCAGACCTGAATCCCTCTCTGCA (FRMD1), mRNA ACTCCTGTTTGCAAGCGCTGGGCCTGCC (SEQ ID NO: 552) 14 2 RBC A_24_P102343 NM_017957 EPN3 Homo sapiens epsin 3 (EPN3), mRNA TCCCTCAGCTTCCTCCTTGGTCAACCTTGACT CGTTGGTCAAGGCACCCCAGGTTGCAAA (SEQ ID NO: 553) 14 A_24_P233078 NM_021093 PYY2 Homo sapiens peptide YY, 2 (seminalplasmin) GCCCACCTCATTTACATGTTCACTCCCGACCC (PYY2), mRNA TGGAAACCCGGATTTCGCCTCCGGACAG (SEQ ID NO: 554) 14 4 RBC A_24_P256083 HS526I14 Human DNA sequence from clone RP3-526I14 on ATTTTCACCTCCCCTGGTCCATGCTCAGGAAG chromosome 22, complete sequence. TCTGGTCACCCTGGCAAACTGCACCTGA (SEQ ID NO: 555) 14 3 RBC A_24_P318990 HSZ85332 H. sapiens Ig lambda light chain variable region TCTGACACCTCAGCCTCCCTGGCCATCACTGG gene (22-21SWIA31) rearranged; Ig-Light- ACTCCAGGCTGAAGATGAGGCTGATTAT (SEQ Lambda; VLambda. ID NO: 556) 14 4 RBC A_24_P365523 NM_021784 FOXA2 Homo sapiens forkhead box A2 (FOXA2), CCTCCTACTACCAGGGGGTGTACTCCCGGCC transcript variant 1, mRNA CATTATGAACTCCTCTTAAGAAGACGACG (SEQ ID NO: 557) 14 A_24_P493646 AP002776 Homo sapiens genomic DNA, chromosome 11 TCGCCACGCCAGCCCCTTTCCTCAGAACGCC clone: RP11-126P21, complete sequence. GAGGCCTCAGGAGCGTGTGCGCGCCGGGA (SEQ ID NO: 558) 14 2 RBC A_24_P911718 AF240580 Homo sapiens clone 17ptel_2111ctg_drft CTTCCTTCCCTAGGATCTCAGCACCCTTTTAGA sequence. TCCCGTGCAGATTGTCTTTCTGTTAAA (SEQ ID NO: 559) 14 A_24_P920188 AY236488 Homo sapiens unidentified genomic region, partial CTCCTTCCCCATCTTCTGGTAACACAACCTTTA sequence. TTTATTTGTGGGGAACCTATTCCCTGT (SEQ ID NO: 560) 14 6 RBC A_32_P48536 2772567 7n93b04.x1 NCI_CGAP_Ov18 Homo sapiens AATTGCCATGCTGCCCACCTCCCGAAGTGTTA cDNA clone IMAGE: 3571927 3′, mRNA sequence GGAGGTAACATCTCATCGTCTCATCGCA (SEQ ID NO: 561) 15 all cell types 15 A_23_P101121 NM_031303 KATNAL2 Homo sapiens katanin p60 subunit A-like 2 TCAGAAGATCTCGTATTTGTCTTAGCAGCTTCT (KATNAL2), mRNA AACCTGCCGTGGTAAGAGACCAAGAGA (SEQ ID NO: 562) 15 A_23_P120243 NM_024501 HOXD1 Homo sapiens homeobox D1 (HOXD1), mRNA TTTTTTCTTTAAAAAAGCGGTTTCTACCTCTCTA TGTGCCTGAGTGATGATACAATCGCT (SEQ ID NO: 563) 15 A_23_P132845 NM_004366 CLCN2 Homo sapiens chloride channel 2 (CLCN2), mRNA TGGGAGTGGACCATGCTTATGTCACCAGTATT GGCAGACTCATTGGAATCGTTACTCTAA (SEQ ID NO: 564) 15 A_23_P15765 NM_018996 TNRC6C Homo sapiens trinucleotide repeat containing 6C GACATTGTGTTTGCAACATGGGCCTCTTATCA (TNRC6C), mRNA CATTCCACCTGAATCTGACTCAAGGCAA (SEQ ID NO: 565) 15 A_23_P313623 NM_015198 COBL Homo sapiens cordon-bleu homolog (mouse) GTCTACAGGCCAAAATGCGCACAGTTGATTT (COBL), mRNA CGGTGTGTTCCTGTATAACGGCTTGAAA (SEQ ID NO: 566) 15 A_23_P319466 NM_020377 CYSLTR2 Homo sapiens cysteinyl leukotriene receptor 2 GGCAAATAGCAAAAGTTGTTGCACTCCTGAAA (CYSLTR2), mRNA TTCTATTAACATTTCCGCAGAAGATGAG (SEQ ID NO: 567) 15 A_23_P369994 NM_004734 DCAMKL1 Homo sapiens doublecortin and CaM kinase-like 1 AAATGTTTTTACCGTAGCCCTCATCTAACTTAC (DCAMKL1), mRNA ACGTGGTGCATATTAAAATAAGCAGAG (SEQ ID NO: 568) 15 A_23_P39294 AC011533 Homo sapiens chromosome 19 clone LLNLR- CTCCCAGCAGAGTCATCACTACCTTTGGGGCC 240E6, complete sequence. GCAGGATCACCCAGCTTGGAACTAGATA (SEQ ID NO: 569) 15 A_23_P399797 AC009014 Homo sapiens chromosome 5 clone P1_748D6, ACAACTGCCCAGAGTGTAATTCCCACCGATAA complete sequence. GCGCGGATCCTTATCTTTGAAACACAAA (SEQ ID NO: 570) 15 A_23_P413923 NM_022160 DMRTA1 Homo sapiens DMRT-like family A1 (DMRTA1), CTGTACTTCAGACCAAATCAGGACAATCCGTA mRNA ATGTATATGCCCATTCTCTCTTTCTGGA (SEQ ID NO: 571) 15 A_23_P45560 NM_000273 GPR143 Homo sapiens G protein-coupled receptor 143 ATATTCCTCAGACTCAACAATTCTTGTTCTTTA (GPR143), mRNA GAACTGTGTTCTCACCTTCCCAACACT (SEQ ID NO: 572) 15 A_23_P502413 NM_002974 SERPINB4 Homo sapiens serpin peptidase inhibitor, clade B TCCTCTTCTATGGCAGATTCTCATCCCCATAGA (ovalbumin), member 4 (SERPINB4), mRNA TGCAATTAGTCTGTCACTCCATTTAGA (SEQ ID NO: 573) 15 A_23_P81103 NM_003013 SFRP2 Homo sapiens secreted frizzled-related protein 2 ATAACCTACATCAACCGAGATACCAAAATCATC (SFRP2), mRNA CTGGAGACCAAGAGCAAGACCATTTAC (SEQ ID NO: 574) 15 A_24_P20091 NM_153041 FLJ32955 Homo sapiens hypothetical protein FLJ32955 CACAAATTCCTCACTCATCTTGCAGAAGCTCC (FLJ32955), mRNA CAGTTTTCAATATTCTCCTAAATGCTGT (SEQ ID NO: 575) 15 A_24_P252780 NM_198514 NHLRC2 Homo sapiens NHL repeat containing 2 GTTCCTAGTAGAAAAACAGAAGACATTACCCA (NHLRC2), mRNA AACTACCTAAATCTGCTCCAAGCATTAG (SEQ ID NO: 576) 15 A_24_P382187 NM_001552 IGFBP4 Homo sapiens insulin-like growth factor binding GAAAAATCTCATTCCCAGAGTCAGAGGAGAAG protein 4 (IGFBP4), mRNA AGACATGTACCTTGACCATCGTCCTTCC (SEQ ID NO: 577) 15 A_24_P410605 BC080541 Homo sapiens receptor tyrosine kinase-like orphan GACATCCCAGCTTGCGGTAAATAGAAGTCATT receptor 1, mRNA (cDNA clone IMAGE: 5477978), GCCCCTAATGTATTCAATCATCTTTAAA (SEQ complete cds. ID NO: 578) 15 A_24_P499215 NM_001005751 LOC387680 Homo sapiens similar to KIAA0592 protein TCAAAGACAAGAGAAAGCAAAAGCCTCCAAGC (LOC387680), mRNA TCTCCAAAAAGAAAGCATCTGCCCTGTT (SEQ ID NO: 579) 15 A_24_P744957 AL353653 Human DNA sequence from clone RP11-244L4 on AGACACAGGATGTTCCTGTTGGTCCAGATACT chromosome 20 Contains ESTs, STSs and GSSs, TGAGCTAAAAGGTGATGGATACCTGGAT (SEQ complete sequence. ID NO: 580) 15 A_24_P82155 NM_182703 ANKDD1A Homo sapiens ankyrin repeat and death domain CTACTTCCCAAAATAGTATTTCTCTCAGCAGAT containing 1A (ANKDD1A), mRNA ATTTCTTTGGTACTACCATGTATTGTG (SEQ ID NO: 581) 15 A_24_P91165 NM_000723 CACNB1 Homo sapiens calcium channel, voltage- TACTTCAAAGGCTCATCAAGTCCCGAGGAAAG dependent, beta 1 subunit (CACNB1), transcript TCTCAGTCCAAACACCTCAATGTCCAAA (SEQ variant 1, mRNA ID NO: 582) 15 A_24_P933902 AY358788 Homo sapiens clone DNA129793 AVLL5809 TCGCGGTGAGACTGAACATTTCATGAGCTCAT (UNQ5809) mRNA, complete cds. GTTGCCTTTGACCACCATTTCTTAAGGA (SEQ ID NO: 583) 15 A_24_P934063 NM_004978 KCNC4 Homo sapiens potassium voltage-gated channel, ATGGGAGATTTTCCACCAGTCCTGTGCAAACA Shaw-related subfamily, member 4 (KCNC4), AGGATATCTGAGTCTTTCCCAGCGAAAA (SEQ transcript variant 1, mRNA ID NO: 584) 15 A_32_P102383 HS243L18 Human DNA sequence from clone RP1-243L18 on TTCTCTTGAGGGTTGAGAGAGTCTGTTTTCCT chromosome 1p36.11-36.23 Contains the 5′ end of AAGAATCTGGTTCTCTCCATCAGTCTCT (SEQ a novel gene (KIAA1026) and a CpG island, ID NO: 585) complete sequence. 15 A_32_P146764 AC002076 Homo sapiens BAC clone GS1-345D13 from 7, ATGTCTCTTTCAACCATATGATCAATCAGTTGG complete sequence. ACGACTTCTGGTTTTTCCTGAATAAAT (SEQ ID NO: 586) 15 A_32_P181131 NM_001005353 AK3L1 Homo sapiens adenylate kinase 3-like 1 (AK3L1), CTCTTCATAGCTCAGTTCTCAGTGCATACAGA nuclear gene encoding mitochondrial protein, GATTCAATATAGCCCCATCGCTCTCAGT (SEQ transcript variant 1, mRNA ID NO: 587) 15 A_32_P221507 BC066346 Homo sapiens cDNA clone IMAGE: 4824446, CATAGAGCAGTTGCTCCCCATTGACACCAAGT partial cds. AATTCCAGTCCACATTTGCCTTTAAGCA (SEQ ID NO: 588)

TABLE 2 Corre- lation- Feature Agilent Probe Gene Description IFI27 Sequence 2703 A_23_P48513 IFI27 interferon, alpha- 1 ACCCAGCGAGGAGCCAACTATCCCAAATATACCTGGG inducible protein GTGAAATATACCAAATTCTGCAT (SEQ ID NO: 589) 27 variant a 40154 A_23_P48513 IFI27 interferon, alpha- 0.999 ACCCAGCGAGGAGCCAACTATCCCAAATATACCTGGG inducible protein GTGAAATATACCAAATTCTGCAT (SEQ ID NO: 590) 27 variant a 32566 A_23_P48513 IFI27 interferon, alpha- 0.999 ACCCAGCGAGGAGCCAACTATCCCAAATATACCTGGG inducible protein GTGAAATATACCAAATTCTGCAT (SEQ ID NO: 591) 27 variant a 7079 A_23_P48513 IFI27 interferon, alpha- 0.999 ACCCAGCGAGGAGCCAACTATCCCAAATATACCTGGG inducible protein GTGAAATATACCAAATTCTGCAT (SEQ ID NO: 592) 27 variant a 508 A_23_P48513 IFI27 interferon, alpha- 0.999 ACCCAGCGAGGAGCCAACTATCCCAAATATACCTGGG inducible protein GTGAAATATACCAAATTCTGCAT (SEQ ID NO: 593) 27 variant a 18306 A_23_P48513 IFI27 interferon, alpha- 0.999 ACCCAGCGAGGAGCCAACTATCCCAAATATACCTGGG inducible protein GTGAAATATACCAAATTCTGCAT (SEQ ID NO: 594) 27 variant a 5149 A_23_P48513 IFI27 interferon, alpha- 0.999 ACCCAGCGAGGAGCCAACTATCCCAAATATACCTGGG inducible protein GTGAAATATACCAAATTCTGCAT (SEQ ID NO: 595) 27 variant a 13333 A_23_P48513 IFI27 interferon, alpha- 0.998 ACCCAGCGAGGAGCCAACTATCCCAAATATACCTGGG inducible protein GTGAAATATACCAAATTCTGCAT (SEQ ID NO: 596) 27 variant a 6656 A_24_P270460 IFI27 interferon, alpha- 0.997 TGAAATATACCAAATTCTGCATCTCCAGAGGAAAATAA inducible protein GAAATAAAGATGAATTGTTGCA (SEQ ID NO: 597) variant a 16373 A_23_P48513 IFI27 interferon, alpha- 0.996 ACCCAGCGAGGAGCCAACTATCCCAAATATACCTGGG inducible protein GTGAAATATACCAAATTCTGCAT (SEQ ID NO: 598) 27 variant a 5290 A_23_P48513 IFI27 interferon, alpha- 0.996 ACCCAGCGAGGAGCCAACTATCCCAAATATACCTGGG inducible protein GTGAAATATACCAAATTCTGCAT (SEQ ID NO: 599) 27 variant a 27987 A_23_P819 G1P2 interferon, alpha- 0.911 CACGGTCCTGCTGGTGGTGGACAAATGCGACGAACCT inducible protein CTGAGCATCCTGGTGAGGAATAA (SEQ ID NO: 600) 27626 A_23_P45871 IFI44L chromosome 1 ORF 29 0.893 TTGTTCGTTTTGCCTTCTGTCCTTGGAACAGTCATATCT (C1orf29) CAAGTTCAAAGGCCAAAACCT (SEQ ID NO: 601) 11715 A_32_P132206 USP18 ubiquitin specific 0.887 AGACTTGTATACTGGCTGAATATCAGTGCTGTTTGTAA protease 18 TTTTTCACTTTGAGAACCAACA (SEQ ID NO: 602) 21005 A_24_P28722 RSAD2 viperin (cig5) 0.877 ACTCTGAGTCAGTTGAAATAGGGTACCATCTAGGTCAG TTTAAGAAGAGTCAGCTCAGAG (SEQ ID NO: 603) 30386 A_24_P261929 FAM14B family with sequence 0.868 TGCAGTCAGTGGGGGCAGCTGGACTCTCTGTGACATC similarity 14, TAAAGTTATCGGGGGCTTTGCTG (SEQ ID NO: 604) member B 36995 A_32_P99533 G1P2 interferon, alpha- 0.864 ACCAGGATGTTCAGAGGTTCGTCGCATTTGTCCACCA inducible protein CCAGCAGGACCGTGCTGCCGGGG (SEQ ID NO: 605) 36654 A_24_P361896 MT2A metallothionein 2A 0.863 CGCTCCCAGATGTAAAGAACGCGACTTCCACAAACCT GGATTTTTTATGTACAACCCTGA (SEQ ID NO: 606) 21017 A_24_P316965 RSAD2 viperin (cig5) 0.861 ATTCTGGATGAATATATGCGCTTTCTGAACTGTAGAAA GGGACGGAAGGACCCTTCCAAG (SEQ ID NO: 607) 12478 A_23_P64828 QAS1 2′,5′-oligoadenylate 0.855 CTCTGCATCTACTGGACAAAGTATTATGACTTTAAAAAC synthetase 1 variant CCCATTATTGAAAAGTACCTG (SEQ ID NO: 608) E18 36260 A_23_P106844 MT2A metallothionein 2A 0.854 CAACCCTGACCGTGACCGTTTGCTATATTCCTTTTTCT ATGAAATAATGTGAATGATAAT (SEQ ID NO: 609) 16580 A_23_P23074 IFI44 interferon-induced 0.852 AAGGATGTTCTAATTCTTTCTGCTCTGAGACGAATGCT protein 44 ATGGGCTGCAGATGACTTCTTA (SEQ ID NO: 610) 22208 A_23_P252413 MT2A metallothionein 2A 0.850 CTGACCGTGACCGTTTGCTATATTCCTTTTTCTATGAAA TAATGTGAATAATAATTAAAC (SEQ ID NO: 611) 20525 A_23_P201459 G1P3 interferon, alpha- 0.846 AGTAGCCAGCAGCTCCCAGAACCTCTTCTTCCTTCTTG inducible protein GCCTAACTCTTCCAGTTAGGAT (SEQ ID NO: 612) variant 43723 A_23_P105794 EPSTI1 epithelial stromal 0.846 AGAAGAGAAGCATTTAGAGAGCATCAGCAATACAAAAC interaction 1 CGCTGAGTTCTTGAGCAAACTG (SEQ ID NO: 613) 16830 A_24_P316257 FLJ36208 hypothetical protein 0.839 TGGGGGAGCTTCCTACAAGGAGAGACTCCTGCTGCTT FLJ36208 TGGAAAACTGAGAAAAAATAGGG (SEQ ID NO: 614) 25919 A_23_P131255 DNAPTP6 DNA polymerase-trans- 0.836 CTGAAGATCAGAGGCTCAGTTAGCAACCTGTGTTGTA activated protein 6 GCAGTGATGTCAGTCCATTGATT (SEQ ID NO: 615) 41211 A_32_P227059 RSAD2 upsteam 5′ end of Gene 0.835 CAAAATAATCTGAAACTTTACTGGCCAAAGTGGGACTC CTTTAAAATTCCAAAACTTGCC (SEQ ID NO: 616) 41347 A_23_P384355 LOC129607 thymidylate kinase 0.834 ACAGTGGATCTTGGAGTGGGATTTCTTGGGTAAATTAT family LPS-inducible CTTTGCCCTTTGAAATGTCTCC (SEQ ID NO: 617) member 36358 A_23_P47955 QAS3 2′-5′ oligoadenylate 0.834 AGAAGGCAGAGAAAGTGAAGACCAAGTCCAGAACTGA synthetase 3 ATCCTAAGAAATGCAGGACTGCA (SEQ ID NO: 618) 14388 A_24_P335305 OAS3 2′-5′ oligoadenylate 0.833 TCTTTGGCAATGGCCACCCTGGTGTTGGCATATTGGC synthetase 3 CCCACTGTAACTTTTGGGGGCTT (SEQ ID NO: 619) 19864 A_24_P943205 EPSTI1 downstream from gene 0.824 AACCAAATATCTATGTAGGCAGAGGTAACCAGGAGAG AAGCAAGACTTGCTGCCTAAAGG (SEQ ID NO: 620) 3173 A_23_P132159 USP18 ubiquitin specific 0.822 CTGTCATTTTCCATTTCCGTTCCTGGATCTACGGGAGTC protease 18 TTCTAAGAGATTTTGCAATGAG (SEQ ID NO: 621) 23814 A_23_P139786 OASL 2′-5′-oligoadenylate 0.821 GTTTCCAGCCAGTTAGTTTTCTCTGGGAGACTTCTCTG synthetase-like TACATTTCTGCCATGTACTCCA (SEQ ID NO: 622) variant 28716 A_24_P557479 HSXIAPAF1 XIAP associated fac- 0.816 CAAATAAACCAACGGGAAAAAAGAAAGGTTCCAGTTTT tor-1 variant 2 GTCTGAAAATTCTGATTAAGCC (SEQ ID NO: 623) 39451 A_23 P206724 MT1E metallothionein 1E 0.816 GGCATGGGAGAAGTGCAGCTGCTGTGCCtGATGTGG GAAGAGCTCTTCTCCCAGATGTAA (SEQ ID NO: 624) 632 A_23_P52266 IFIT1 interferon-induced 0.815 ACTTTGAGAACTCTGTGAGACAAGGTCCTTAGGCACC protein variant 2 GAGATATCAGCCACTTTCACATT (SEQ ID NO: 625) 7680 A_23 P427703 MT1E 602705675F1 NIH_MGC_43 0.813 CTGCTGTGCCTGATGTGGGGACAGACCTGCTCCCAGG clone IMAGE: 4842259 TGTAAACAGAGCAACCTGCACAA (SEQ ID NO: 626) 5′ 18216 A_23_P17663 MX1 myxovirus (influenza 0.808 CAGCTTATTTGCTCATTTTTATAATGTCCCTTCACAAAC virus) resistance 1, CCAGTGTTTTAGGAGCATGAG (SEQ ID NO: 627) IFI protein p78 1309 A_23_P303242 MT1X metallothionein 1x 0.805 TGCCAAGTGTGCCCAGGGCTGCATCTGCAAAGGGAC GTCAGACAAGIGCAGCTGCTGTGC (SEQ ID NO: 628) 13366 A_23_P414343 MT1J metallothionein 1J 0.804 TGTGCCAAGTGTGCCCACGGCTGCATCTGCAAAGGGA CGTCGGAGAAGTGCAGCTGCTGT (SEQ ID NO: 629) 21994 A_23_P60933 MT1G metallothionein 1G 0.804 AGCTGCTGTGCCTGATGTCGGGACAGCGCTGCTCCCA AGTACAAATAGAGTGACCCGTAA (SEQ ID NO: 630) 22827 A_23_P166797 IFRG28 28kD interferon re- 0.798 CAAGCAGGATCAAGTTTGTAGAATAAACACTGGTTTCC sponsive protein TAGCCATCCTCTGAAAACAGTA (SEQ ID NO: 631) 34047 A_24_P317762 LY6E lymphocyte antigen 6 0.798 CTACTGCGTGACTGTGTCTGCTAGTGCCGGCATTGGG complex, locus E AATCTCGTGACATTTGGCCACAG (SEQ ID NO: 632) 27981 A_23_P4286 HSXIAPAF1 XIAP associated fac- 0.796 TTTAACAGTGGCATTCCTGCCTACTTGCTGTGGTGGTC tor-1 variant 2 TTGTGAAAGGTGATGGGTTTTA (SEQ ID NO: 633) 41919 A_24_P917810 BRCA2 BRCA2 intron 0.795 TTTGCACTATGGTAGATTTCAGGAATTTCAAAAGAAATC intron TGATGTCAGTGCAATTATCCG (SEQ ID NO: 634) 42276 A_23_P4283 BIRC4BP X-linked inhibitor 0.791 TCAACTTGACTTCATGTTAAAAACCCTCAACAAACCAG of apoptosis GCGTCGAAGGAACATACCTCAA (SEQ ID NO: 635) 7108 A_23_P204087 OAS2 2′-5′-oligoadenylate 0.789 TCTTCAAAGCAAAGCTCTTTACTTTCCCCTTGGTTCTCA synthetase 2 variant 1 TAACTCTGTGATCTTGCTCTC (SEQ ID NO: 636) 8777 A_23_P110196 HERC5 hect domain and RLD 5 0.787 TGTCCTGAAAGTTGGAATGAAAGAGACCCTATAAGAG CACTGACATGTTTCAGTGTCCTC (SEQ ID NO: 637) 1565 A_24_P343929 OAS2 2′-5′-oligoadenylate 0.784 GGAAGGTCAATTACAACTTTGAAGATGAGACCGTGAG synthetase 2 variant 1 GAAGTTTCTACTGAGCCAGTTGC (SEQ ID NO: 638) 18175 A_23_P35412 IFIT4 IFI protein with 0.779 ATTCGAATAAAGCTCTTGAGAAGGGACTGAATCCTCTG tetratricopeptide re- AATGCATACTCCGATCTCGCTG (SEQ ID NO: 639) peats 4 18624 A_23_P38346 LGP2 likely ortholog of 0.775 CATACTGTACTCAGAATCACGACATTCCTTCCCTACCA mouse D11Igp2 AGGCCACTTGTATTTTTTGAGG (SEQ ID NO 640) 28011 A_23_P250353 HERC6 hect domain and RLD 6 0.764 TTTCACCTCAGTCTGTAATTGGCTGTGAGTCAGTCTTTC ATTTACATAGGGTGTAACCATC (SEQ ID NO: 641) 24371 A_23_P37983 MT1B metallothionein 1B 0.761 TCATCAGAGAAGTGCCGCTGCTGTGCCTGATGTTGGG AGAGCCCTGCTCCCAGACATAAA (SEQ ID NO: 642) 18869 A_24_P378019 IRF7 interferon regulatory 0.760 CAACAGCCTCTATGACGACATCGAGTGCTTCCTTATGG factor variant a AGCTGGAGCAGCCCGCCTAGAA (SEQ ID NO: 643) 11320 A_24_P125096 MT1X metallothionein 1X 0.759 CCAGGGCTGCATGTGCAAAGGGACGTCAGACAAGTGC AGCTGCTGTGCCTGATGCCAGGA (SEQ ID NO: 644) 20855 A_23_P152782 IFI35 interferon-induced 0.758 CGGAAGTGCCTAAGTCTTTAGTTTCCAATTTGCGGATC protein 35 CACTGCCCTCTGCTTGCGGGCT (SEQ ID NO: 645) 33108 A_32_P15128 OAS2 2′-5′-oligoadenylate 0.755 TAAAGAGCTTTGCITIGAAGACACAGAGGATTCCTTTT synthetase 2 variant 1 TTAGACTGGAAGGAAAAAGGAG (SEQ ID NO: 646) 40042 A_24_P30194 IFIT5 IFI protein with 0.741 AATGTGGCTTCTCTAATGTAGTTTCTTTGATTACCGACT tetratricopeptide re- ACACAATTATGTACCATCACA (SEQ ID NO: 647) peats 5 7065 A_23_P132388 SCO2 SCO cytochrome oxidase 0.738 AGTCACAGTTACCGCGTGTACTACAATGCCGGCCCCA deficient homolog 2 AGGATGAGGACCAGGACTACATC (SEQ ID NO: 648) 4620 A_23_P63668 IFIT5 IFI protein with 0.731 AAGATAGATCCAGAAAATGCAGAATTCCTGACTGCTCT tetratricopeptide re- CTGTGAGCTCCGACTTTCCATT (SEQ ID NO: 649) peats 5 32013 A_23_P38894 FLJ11286 hypothetical protein 0.727 ATCCCCCCACCAGGATAAAAGTCCTGACCTTTGTTCTC FLJ11286 TTGACGGAATAAAAGCTTGCTT (SEQ ID NO: 650) 41755 A_23 P29773 LAMP3 lysosomal-associated 0.726 ACCATGTTGACTTTCCTCATGTGTTTCCTTATGACTCAG membrane protein 3 TAAGTTGGCAAGGTCCTGACT (SEQ ID NO: 651) 3171 A_23_P64343 TIMM10 translocase of inner 0.725 ATGAGCGGATGGGCAAAAAGTTGACAGAGTTGTCTAT mitochondrial membrane GCAGGATGAAGAGCTGATGAAGA (SEQ ID NO: 652) 10 homolog 35302 A_23_P39465 BST2 bone marrow stromal 0.722 TGCTCGGCTTTTCGCTTGAACATTCCCTTGATCTCATC cell antigen 2 AGTTCTGAGCGGGTCATGGGGC (SEQ ID NO 653) 28820 A_23P_370682 MGC20410 hypothetical protein 0.722 TGGAAGTTCAGTTTTGGTGTCTGCTTCAAGAGGGGGT BC012330 TTTACACTCTGATTCCAGGACAA (SEQ ID NO: 654) 16269 A_23_P358944 PML promyelocytic leukemia 0.718 GGACTGGCTATCCCAAGACCTGGCAGATGTGGCTGCT variant 8 CAATAAACACTTGTTGAACCATC (SEQ ID NO: 655) 13700 A_23_P142750 PRKR protein kinase, IFI 0.717 AGAACAGATTTCTTCGCAAGACTATGGAAAGGAAGTG double-stranded RNA GACCTCTACGCTTTGGGGCTAAT (SEQ ID NO: 656) dependent 26554 A_23_P259141 DLM-1 FLJ46548 fis, 0.716 ATGTTTGAGTCCCAACAAAATTCATATCAAAACATAATC THYMU3038347, highly CCAACTGGGTGCAGTGGCTCA (SEQ ID NO: 657) similar to DLM-1 7372 A_32_P54553 USP41 ubiquitin specific 0.714 ATATGATCCGGATGAAGGACTCCTTGATTTGCCTTGAC protease 41 TGTGCCATGGAGAGTAGCAGAA (SEQ ID NO: 658) 22061 A_24_P334361 FLJ20035 hypothetical protein 0.712 GTGAAAATGAAGACGACAACGTTGTCTTAGCCTTTGAA FLJ20035 CAACTGAGTACAACTTTTTGGG (SEQ ID NO: 659) 23517 A_23_P139123 SERPING1 serine proteinase in- 0.710 GACAACATTTGATCCCAAGAAAACCAGAATGGAACCCT hibitor, clade G TTCACTTCAAAAACTCAGTTAT (SEQ ID NO: 660) member 1 19683 A_32_P452655 LGALS9 lectin, galactoside- 0.708 TGACCAGAGTGTTCTCTTCAGGGGACTGGCTCCTTTC binding, soluble, 9 CCAGTGTCCTTAAAATAAAGAAA (SEQ ID NO: 661) variant 28706 A_23_P218879 TREX1 three prime repair 0.707 CAGCCTTGGAGAGAGCAGGGGTACCAAGGATCTTCCT exonuclease 1 variant CCAGTGAAGGACCCTGGAGCCCT (SEQ ID NO: 662) 4 41524 A_24_P332926 SFRS14 splicing factor, argi- 0.701 GTGTGTCTCATCCAGGAGCCAAAAGTCCATGAACCAG nine/serine-rich 14 TTCGAATTGCCTATGACAGGCCT (SEQ ID NO: 663) 3797 A_23_P20814 DDX58 DEAD (Asp-Glu-Ala-Asp) 0.697 TGAGTGGAGAAGAAACAAACATAGTGGGTATAATCAT box polypeptide 58 GATCGCTTGTACCCCTGTGAAA (SEQ ID NO: 664) 40576 A_32_P134290 ZCCHC2 zinc finger, CCHC 0.697 AATTAATTGTTAAGCTGCAGTTGAGTTGTTCAAGTGAG domain containing 2 AGTTTTGATAAGCCACTTATGG (SEQ ID NO: 665) 8270 A_23P_145874 C7orf6 chromosome 7 ORf 6 0.695 CATTGATATCCACTGGTCACATCATAACTGTCTATAGG GCAATAAAATCTGTGTTAAACT (SEQ ID NO: 666) 10995 A_23_P304054 LOC400653 hypothetical LOC400653 0.694 AGTTCTTTACGCTTTCTGATTGAACTGATTTGAAGTTCT TATTTCGTGTGTTGGGGAACA (SEQ ID NO: 667) 23236 A_23_P68155 MDA5 melanoma differentia- 0.693 CTACGTCCTGGTTGCTCACAGTGGTTCAGGAGTTATC tion associated pro- GAACGTGAGACAGTTAATGATTT (SEQ ID NO: 668) tein-5 40635 A_23_P206441 FANCA Fanconi anemia, com- 0.685 ATGAGGGCCTCGTTTATTAAGATCTTTAAACTGCTTTAT plementation group A ACACTGTCACGTGGCTTCATC (SEQ ID NO: 669) 43149 A_23_P17481 SIGLEC1 lectin-like adhesion 0.681 GGAAGAGGTGATCACTCTCACACTAAGACTGAGGAAA molecule TAAAAAAGGTTTGGTGTTTTCCT (SEQ ID NO: 670) 1523 A_24_P561165 SERPING1 serine proteinase in- 0.678 CGATTTTTCTTCATGACCTTAACCTGTGTGGGCTAACA hibitor, clade G member 1 GAGGACCCAGATCTTACAGGTT (SEQ ID NO: 671) 34907 A_23_P111804 ZC3HDC1 zinc finger CCCH type 0.677 TGATTCGGTTTCTCAGAGTCTCATGGCATCATAGTTTTT domain containing 1 CCAGAATGACACAGTAGCCAC (SEQ ID NO: 672) 37561 A_24_P304071 IFIT2 IFI protein with 0.673 TCTAAGAGAGAATGGAATGTATGGGAAAAGAAAGTTAT tetratricopeptide TGGAACTAATAGGACACGCTGT (SEQ ID NO. 673) repeats 2 37323 A_24_P118892 IRF7 interferon regulatory 0.669 TCAGCCGGGAGCTGTGCTGGCGAGAAGGCCCAGGCA factor 7 variant a CGGACCAGACTGAGGCAGAGGCCC (SEQ ID NO: 674) 1157 A_23_P163782 MT1H metallothionein 1H 0.668 AAGTGCAAATGCACCTCCTGCAAGAAGAGCTGCTGCT CCTGTTGCCCCCTGGGCTGTGCC (SEQ ID NO: 675) 21378 A_23_P97064 FBXO6 F-box protein 6 0.665 CAACAGTGGAACAATGCCACATGGACAGAGGTCTCCT ACACCTTCTCAGACTACCCCCGG (SEQ ID NO: 676) 37891 A_23_P18604 LAP3 leucine aminopeptidase 0.660 TTCGTTTCAGTCAAGACAATGCTTAGTTCAGATACTCA 3 AAAATGTCTTCACTCTGTCTTA (SEQ ID NO: 677) 1986 A_23_P69109 PLSCR1 phospholipid scram- 0.660 GTTTAGCTCTTACACTCTATCCTTCCTAGAAAATGGTAA blase 1 TTGAGATTACTCAGATATTAA (SEQ ID NO: 678) 6936 A_23_P203498 TRIM22 tripartite motif-con- 0.652 GTACATAAGAATCTATCACTAAGTAATGTATCCTTCAGA taining 22 ATGTGTTGGTTTACCAGTGAC (SEQ ID NO: 679) 17172 A_23_P120435 WFDC3 WAP four-disulfide 0.652 ACCAGTCCTGCCCCCAAAACTGACCATGAACCCCAAC core domain 3 variant TGGACTGTGAGGTCTGATTCCGA (SEQ ID NO: 680) 4 7518 A_23_P21838 CNP 2′,3′-cyclic nucleo- 0.651 TAACAGGGCCTTGCTAATCGGGTTGTCACTCAAC tide 3′ phosphodi- GTGCTTTGGATTTAAGTTACTA (SEQ ID NO: 681) esterase 36793 A_32_P156746 STAT2 signal transducer and 0.651 GAGATTGTCCAGAGTCCTATGACAGACCTTCAAGGTTT activator of tran- TAAGTTCCACAGACTTGGACTT (SEQ ID NO: 682) scription 2 22443 A_23_P209995 IL1RN interleukin 1 receptor 0.646 TATTCCTGCATTTGTGAAATGATGGTGAAAGTAAGTGG antagonist variant 4 TAGCTTTTCCCTTCTTTTTCTT (SEQ ID NO: 683) 23150 A_23_P161125 MOV10 Moloney leukemia virus 0.642 TCCCCGTACCGGAAACAGGTGGAGAAAATCCGTTACT 10, homolog GCATCACCAAACTTGACAGGGAG (SEQ ID NO: 684) 17566 A_24_P395966 ZBP1 Z-DNA binding protein 0.641 GTCGTCGTCCCGCAGACACACAATCCAGAAGTCACTT 1 TCCTCGAGACATTGGTCAGCCCA (SEQ ID NO: 685) 8222 A_23_P250358 HERC6 hect domain and RLD 6 0.639 CCTTACACCTAAATAATACAAGAGATTAATGAATAGTG GTTAGAAGTAGTTGAGGGAGAG (SEQ ID NO: 686) 41451 A_24_P172481 TRIM22 tripartite motif-con- 0.639 TGCCCCTTAAAAGATTGAAGAAAGAGAAACTTGTCAAC taining 22 TCATATCCACGTTATCTAGCAA (SEQ ID NO: 687) 18011 A_24_P7040 IFITM3 interferon induced 0.636 CGCCAAGCATGTGAACATCTGGGCCCTGACTGTGGGC transmembrane protein ATCCTCATGACCATTCTGCTCAT (SEQ ID NO: 688) 15599 A_24_P117410 LOC113730 hypothetical protein 0.635 GCTCAGGGAAGGGGCTGGGATCGGAACTTCCTGCTCT BC009980 TGTTTCTGGACAACTTTCCCCTT (SEQ ID NO: 689) 2072 A_23_P75741 UBE2L6 ubiquitin-conjugating 0.628 AATAGACCGAATATCAGGGAGCCCCTGCGGATGGACC enzyme E2L 6 variant 2 TCGCTGACCTGCTGACACAGAAT (SEQ ID NO: 690) 37424 A_23_P71148 BLVRA biliverdin reductase A 0.627 AGGTGATGTAGCACTTCCAAGATGGCACCAGCATTTG GTTCTTCTCAAGAGTTGACCATT (SEQ ID NO: 691) 28056 A_24_P45446 GBP4 guanylate binding pro- 0.627 AGGGGACACAGGCTTCTTAAAACAACCCGGCTTCCTC tein 4 ACCCTATGTCCTTTATTTACAAA (SEQ ID NO: 692) 44249 A_23_P101025 LGALS9 lectin, galactoside- 0.622 CCCAGCCTTTCCAACCGTGCCTGGGATCTGGGCTTTA binding, soluble, 9 ATGCAGAGGCCATGTCCTTATCT (SEQ ID NO: 693) variant 24243 A_23_P91802 ECGF1 endothelial cell 0.619 CCGCCTGGGGGTGGGCGGAGAGCTGCTGGTCGACGT growth factor 1 GGGTCAGAGGCTGCGCCGTGGGAC (SEQ ID NO: 694) 3378 A_24_P394246 SCOTIN scotin 0.618 TTCTCTTCCTCACCTGAAATTATGCTTCCTAAAATCTCA AGCCAAACTCAAAGAATGGGG (SEQ ID NO: 695) 17300 A_23_P428248 STI2 TPR domain containing 0.617 GCCATCAACCTACTGAAGTTGTGTGGAGGGATGGAAA STI2 GTGGGTCAGTGGAGAAGGGATTC (SEQ ID NO: 696) 9338 A_23_P24004 IFIT2 IFI protein with 0.615 AGCTGACCCAGCATCAGCCACACTCTGGGTTGGAAAA tetratricopeptide re- TGTTTGCCTGTTGGAATTAATTT (SEQ ID NO: 697) peats 2 28969 A_23_P42353 ETV7 ets variant gene 7 0.611 TGAGCCCTACATCAAGTGGGAAGACAAGGACGCCAAG ATCTTCCGAGTTGTGGATCCAAA (SEQ ID NO: 698) 18692 A_23_P70660 C6orf37 chromosome 6 ORF 37 0.610 GCTATCCGGGTGTTAGCTGACCAAAATGTCATTCCTAA TGTGGCTAATGTCACTTGCTAT (SEQ ID NO: 699) 13508 A_23_P212475 SCOTIN scotin 0.610 ATCTGTTGTGTTTCTGAGTCTAGGGTCTGTACATTGT TTATAATAAATGCAATCGTTTG (SEQ ID NO: 700) 43198 A_23_P216655 TRIM14 tripartite motif-con- 0.609 ATAGCCAGAAAGCGGCAGTTTCAGTCCATATCAATTGT taining 14 variant 1 GTGACCAGGGCTAGTCACTTTT (SEQ ID NO: 701) 8567 A_23_P72737 IFITM1 interferon induced 0.594 ATACAGCAGTTTATACCCACACACCTGTCTACAGTGTC transmembrane ATTCAATAAAGTGCACGTGCTT (SEQ ID NO: 702) protein 1 24307 A_24_P161018 PARP14 poly (ADP-ribose) 0.593 AAATATTPAGATTTCCCTGGACCATAAGAGACCTTTGAT polymerase family, TAAGGTTTTGGGAATTAGGAG (SEQ ID NO: 703) member 14 15588 A_23_P140207 PCK2 phosphoenolpyruvate 0.589 AGGACATAGCACCCTCATCTGGGAATAGGGAAGGCAC carboxykinase 2 CTTGCAGAAAATATGAGCAATTT (SEQ ID NO: 704) 31781 A_32_P38003 EIF2AK2 downstream from gene 0.589 AAACTGTGAGGCAAATAAAATGCTTCTCAAATCTGTGT GGCTCTTATGGGGTTAATTTGA (SEQ ID NO: 705) 27401 A_23_P206441 FANCA Fanconi anemia, com- 0.587 ATGAGGGCCTCGTTTATTAAGATCTTTAAACTGCTTTAT plementation group ACACTGTCACGTGGCTTCATC (SEQ ID NO: 706) A (FANCA) 5503 39922 A_23_P400378 GPBAR1 G protein-coupled bile 0.556 TGTCGACCTGGACTTGAACTAAAGGAAGGGCCTCTGC acid receptor 1 TGACTCCTACCAGAGCATCCGTC (SEQ ID NO: 707) 4393 A_32_P107372 LOC400760 similar to Interferon- 0.585 GGTACTGAGCAGAGTCTTAGGTAAAAGTCTTGGGAAA induced guanylate- TATTTGGGCATTGGTCTGGCCAA (SEQ ID NO: 708) binding protein 1 41600 A_23_P206441 FANCA Fanconi anemia, com- 0.580 ATGAGGGCCTCGTTTATTAAGATCTTTAAACTGCTTTAT plementation group A ACACTGTCACGTGGCTTCATC (SEQ ID NO: 709) 24950 A_23_P121011 AXUD1 AXIN1 up-regulated 1 0.580 GCGTGATGTTCCTTAGCCCAAAGACGGTGAGACAGGG CTGAAATCAGGTGGCTTCTGCCA (SEQ ID NO: 710) 37768 A_23_P206441 FANCA Fanconi anemia, com- 0.577 ATGAGGGCCTCGTTTATTAAGATCTTTAAACTGCTTTAT plementation group A ACACTGTCACGTGGCTTCATC (SEQ ID NO: 711) 26191 A_24_P419286 DNAH3 dynein, axonemal, 0.576 CCCAGAAGATCGTTGCGACCTACCGCCTGTGCTCGGA heavy polypeptide 3 ACAACTGTCCTCTCAGCATCATT (SEQ ID NO: 712) 10783 A_23_P206441 FANCA Fanconi anemia, com- 0.576 ATGAGGGCCTCGTTTATTAAGATCTTTAAACTGCTTTAT plementation group A ACACTGTCACGTGGCTTCATC (SEQ ID NO: 713) 24951 A_23_P15174 MT1F metallothionein 1F 0.573 TGCCAGGACAACCTTTCTCCCAGATGTAAACAGAGAG ACATGTACAAACCTGGATTTTTT (SEQ ID NO: 714) 30864 A_24_P148717 CCR1 chemokine (C-C motif) 0.569 CTTTTCAAGTTGGGTGATATGTTGGTAGATTCTAATGG receptor 1 CTTTATIGCAGCGATTAATAAC (SEQ ID NO: 715) 38267 A_23_P106226 C14orf123 chromosome 14 ORF 123 0.567 CTGAGTGGGTATCCTGATAAATCTGGGCTTGTCTTCCT AATGCTACCTTTGTTGGTCCTT (SEQ ID NO: 716) 40688 A_24_P274270 STAT1 signal transducer and 0.567 TTGAACCCTACACGAAGAAAGAACTTTCTGCTGTTACT activator of tran- TTCCCTGACATCATTCGCAATT (SEQ ID NO: 717) scription 1 variant beta 13093 A_23_P206441 FANCA Fanconi anemia, com- 0.565 ATGAGGGCCTCGTTTATTAAGATCTTTAAACTGCTTTAT plementation group A ACACTGTCACGTGGCTTCATC (SEQ ID NO: 718) 30444 A_24_P344711 AGPAT3 1-acylglycerol-3-phos- 0.565 TCCCATAGAAGTTCCCTCCCTTTGAAATTAATATATAAT phate O-acyltrans- GTATAAATTCTGCACTGAGCC (SEQ ID NO: 719) ferase 3 42135 A_23_P125624 ACATE2 ortholog of acyl-Co- 0.565 TGAAGACCTGATCGAGTGTATTGATTTTAGTATTGCTT enzyme A thioesterase CGTGTCCTGCACACAGGAGGAG (SEQ ID NO: 720) 2, mitochondrial 32604 A_24_P941912 BBAP rhysin 2 0.564 TTTATAATAACGGTAGCCCACATTGTAGTAGTTTTTCAG CTCTTTACTAAGTCCCACCAA (SEQ ID NO: 721) 31047 A_24_P207139 PML promyelocytic leukemia 0.564 ACAGTGAATTTTGATGCATTTAAAATAAGATTCTGATGC variant 1 CAGACTGTTAAAACAGGCGCT (SEQ ID NO: 722) 30304 A_23_P65174 PHF11 PHD finger protein 11 0.564 TATGAAGAAATCGGGAGTGCACTTTTTGACTGTAGATT GTTCGAAGACACATTTGTAAAT (SEQ ID NO: 723) 9201 A_23_P355244 FLJ20073 FLJ20073 protein 0.564 TCACTGGAGGAAGATTTTCCCTTGCTTCTGCATAAAAT (FLJ20073)6853 TTTAACTCCATAACTTATAAGC (SEQ ID NO: 724) 41835 A_23_P69383 BAL B aggressive lymphoma 0.561 TTTTTAGTGGCATGCAGGCTATACCTCAGTATTTGTGG gene ACATGCACCCAGGAATATGTAC (SEQ ID NO: 725) 13417 A_23_P306148 PML promyelocytic leukemia 0.560 AGGCAGAGGAACGCGTTGTGGTGATCAGCAGCTCGG variant 11 AAGACTCAGATGCCGAAAACTCGT (SEQ ID NO: 726) 37690 A_23_P123672 TDRD7 tudor domain contain- 0.560 AAATCTTAACTCTGCTACATGGCTCTGACTGCTGTGGG ing 7 GGATTGAAAAGAATATGCTTAT (SEQ ID NO: 727) 22106 A_23_P6263 LOC442209 FLJ16669 fis, clone 0.555 TCTGGGTCAAATTCTTCTTTTGTATGTCCAGTCTCCTG THYMU30003O6 CACAGCACCTGCAGCATTGTAA (SEQ ID NO: 728) 33663 A_23_P12044 FLJ10199 hypothetical protein 0.554 GCCTGATGAACGTAGGCACGTGATGCGTAATAGTCTT FLJ10199 CAATGGTACACTTAACTAGTCTC (SEQ ID NO: 729) 18942 A_23_P206441 FANCA Fanconi anemia, com- 0.549 ATGAGGGCCTCGTTTATTAAGATCTTTAAACTGCTTTAT plementation group A ACACTGTCACGTGGCTTCATC (SEQ ID NO: 730) 22341 A_23_P423331 NTNG2 netrin G2 0.549 AACTATTTTTGTTTGTATTCACTGTCCCCTGCAAGGGG GACGGGGCGGGAGCACTGGTCA (SEQ ID NO: 731) 39663 A_24_P868905 LOC391020 similar to IFI trans- 0.544 ATCCTCATGAGCATTCTGCTCATCTTCATCCCAGTGTT membrane protein 3 GATCTTTCAAGTCTATCAATAG (SEQ ID NO: 732) 22603 A_32_P92415 PARP14 poly (ADP-ribose) 0.543 GAAGGGTTTCACAATGAAGATGTGTAGCAGGCGTTAT polymerase family, CCCATTGTTATCACTGGGCAGAA (SEQ ID NO: 733) member 14 12663 A_23_P154488 PNPT1 polyribonucleotide 0.543 AAATTCAGGTGAAATACTTTGGACGTGACCCAGCCGAT nucleotidyltransferase GGAAGAATGAGGCTTTCTCGAA (SEQ ID NO: 734) 1 38515 A_24_P15702 EST highly conserved re- 0.542 CCAATGCAGACAAACCACCCCTTTTTGTTGGGAAAGG gion AATTACCTTTGACAGTGGTGGTA (SEQ ID NO: 735) 37436 A_32_P53603 EST space dust 0.542 CTTTTATGTGGTTCCTGCCCCTGAGAATAAAGAAGCCC CAGCGTGGCTGCGAGGCACCAT (SEQ ID NO: 736) 19668 A_23_P116557 LGALS9 lectin, galactoside- 0.542 AGTGTGGATCTTGTGTGAAGCTCACTGCCTCAAGGTG binding, soluble, 9 GCCGTGGATGGTCAGCACCTGTT (SEQ ID NO: 737) variant 31202 A_23_P87545 IFITM3 interferon induced 0.541 GGGCCCTGATTCTGGGCATCCTCATGACCATTCTGCT transmembrane protein CATCGTCATCCCAGTGCTGATCT (SEQ ID NO: 738) 3 39745 A_23_P55564 ZCCHC2 zinc finger, CCHC 0.540 GACATCTGACGTAGAGACCTGCGAATGGATCTGAGAT domain containing 2 GAGTAGTAACGCAGGTTGTCCGG (SEQ ID NO: 739) 31706 A_24_P350124 KIAA1618 KIAA1618 0.540 GCAGATTCTGAGAACAATAACTCCACAATGGCGTCGG CCTCGGAGGGTGAAATGGAGTGT (SEQ ID NO: 740) 31855 A_24_P344087 REC8L1 REC8-like 1 0.539 TCCTGGTGCTCTCAGCGCAACAGATTCTTCACGTGAAA CAAGAAAAGCCATATGGTCGCC (SEQ ID NO: 741) 27231 A_23_P75811 SLC3A2 solute carrier family 0.538 ATCCTGAGCCTACTCGAATCCAACAAAGACTTGCTGTT 3 member 2 GACTAGCTCATACCTGTCTGAT (SEQ ID NO: 742) 35807 A_23_P138856 DRAP1 DR1-associated pro- 0.537 CTTCTGCCCCCCAGACCATAGCCCCTTTTAGTTGGTTT tein 1 (negative TAGTTGCTCTGGGGGGAGGAGA (SEQ ID NO: 743) cofactor 2 alpha) 14385 A_24_P16124 IFITM4P IFI transmembrane pro- 0.536 GGGATTCATAGCATTCACCTACTCCCTGAAGTCTAGG tein 4 pseudogene, GACAGGAAGATGGTTGGAGACCT (SEQ ID NO: 744) chromosome 6 14104 A_23_P62890 GBP1 guanylate binding pro- 0.536 CAAAGATGCATTTACCTCTGTATCAACTCAGGAAATCT tein 1, interferon- CATAAGCTGGTACCACTCAGGA (SEQ ID NO: 745) inducible 21955 A_24_P197964 TRIM14 tripartite motif-con- 0.536 AAATTGCTTGCAGATATTTTTAAATGACAGCAATTTTCT taining 14 variant 4 AATATTTGGTTTAATAAAATG (SEQ ID NO: 746) 23148 A_23_P153372 HSH2D hematopoietic SH2 do- 0.536 GAATCCGAGCCCTTTTCCCATATCATCTGTTTGTTCTG main containing TTGTCTAAAAGCACACTGCAAG SEQ ID NO: 747) 11424 A_23_P206441 FANCA Fanconi anemia, com- 0.532 ATGAGGGCCTCGTTTATTAAGATCTTTAAACTGCTTTAT plementation group A ACACTGTCACGTGGCTTCATC (SEQ ID NO: 748) 8658 A_23_P202964 PORIMIN pro-oncosis receptor 0.531 TCTGAAGCAAAGAAAGGATCAAAATTTGATACTGGGAG inducing membrane CTTTGTTGGTGGTATTGTATTA (SEQ ID NO: 749) injury gene 34298 A_24_P259276 LOC254359 hypothetical protein 0.531 ACTCAGTAAGGAAGTCGGGTTGGACCTTAACATCTGC LOC254359 ATTGGACAACTCCACCCCTTCCT (SEQ ID NO: 750) 26056 A_23_P98167 UNC93B1 unc-93 homolog B1 0.531 TCGCCGGCCTCAGTTTACCACGTCTGAGGTCGGGGG GACCCCCTCCGAGTCCGCGCTGT (SEQ ID NO: 751) 43514 A_32_P157846 FLJ31401 FLJ34941 fis, clone 0.529 ACAGTTGTTTTGTCTTCAAGCCACTGACTTCTGGAATTT NT2RP7007480 GCAGATTTTGCAATCCATGCA (SEQ ID NO 752) 23132 A_24_P50543 LOC400368 hypothetical gene 0.527 AAATCAGCCTCCATCAGTATCACTGCAGTTATATATGA supported by BC031266 TGTATGCCTTATTGCTCAAGAC (SEQ ID NO: 753) 22246 A_23_P214080 EGR1 early growth response 1 0.526 AAACAAAGTGACTGTTTGGCTTATAAACACATTGAATG CGCTTTATTGCCCATGGGATAT (SEQ ID NO: 754) 3490 A_23_P206441 FANCA Fanconi anemia, com- 0.523 ATGAGGGCCTCGTTTATTAAGATCTTTAAACTGCTTTA plementation group A ACACTGTCACGTGGCTTCATC (SEQ ID NO: 755) 2659 A_23_P50108 KNTC2 kinetochore associ- 0.520 AAAGTGGGAAATAACTTGCAACGTCTGTTAGAGATGGT ated 2 TGCTACACATGTTGGGTCTGTA (SEQ ID NO: 756) 21328 A_24_P382319 CEACAM1 carcinoembryonic anti- 0.519 CCATGCTGTGCTGTGTTATTTAATTTTTCCTGGCTAAGA gen-related cell TCATGTCTGAATTATGTATGA (SEQ ID NO: 757) adhesion molecule 1 33919 A_23_P255104 LHFPL2 lipoma HMGIC fusion 0.518 CCAAAAGAGTTAAAGGCACGACTGGGATTTCTTCTGA partner-like 2 GACTGTGGTGAAACTCCTTCCAA (SEQ ID NO: 758) 27245 A_24_P43588 MAD2L1BP MAD2L1 binding protein 0.518 CCATAAACTGACTGTGACCCTGTCATGTGGCAGACCTT variant 1 CCATCCGAACCACGGCTTGGGA (SEQ ID NO: 759) 33581 A_23_P502520 IL4I1 interleukin 4 induced 0.517 CCAGTTATCTCTCCAAAACACGACCCACACGAGGACC 1 variant 2 TCGCATTAAAGTATTTTCGGAAA (SEQ ID NO: 760) 8566 A_24_P54879 SCARB2 scavenger receptor 0.516 AGTGATGTACCTCAATGAGAGTGTTCACATTGATAAAG class B, member 2 AGACGGCGAGTCGACTGAAGTC (SEQ ID NO: 761) 16203 A_24_P175188 FLJ20073 FLJ20073 protein 0.515 TGCCAATGTACTGGCAGATTAACATACAACCTATGTTT TGAACAAAAACAACCAGCGATA (SEQ ID NO: 762) 11310 A_23_P34915 ATF3 activating transcrip- 0.513 GATGTCAATAGCATTGTTTTTGTCATGTAGCTGTTTTAA tion factor 3 GAAATCTGGCCCAGGGTGTTT (SEQ ID NO: 763) 26089 A_23_P75769 MS4A4A membrane-spanning 4- 0.511 CACCAAAAGATCAACAGACAAATGCTCCAGAAATCTAT domains, subfamily A, GCTGACTGTGACACAAGAGCCT (SEQ ID NO: 764) member 4 variant 2 7745 A_23_P166459 LGALS1 lectin, galactoside- 0.511 CCAGATGGATACGAATTCAAGTTCCCCAACCGCCTCA binding, soluble, 1 ACCTGGAGGCCATCAACTACATG SEQ ID NO: 765) 12417 A_32_P71710 IL1RN interleukin 1 receptor 0.510 AAGATTTTATTGTAAAACAGAGCTGAAGTCACAGGAAG antagonist variant 4 TAGGGAACTTTGCACCCAACAT (SEQ ID NO: 766) 35164 A_23_P376488 TNF tumor necrosis factor, 0.509 GGGGTATCCTGGGGGACGCAATGTAGGAGCTGCCTT superfamily member 2 GGCTCAGACATGTTTTCCGTGAAA (SEQ ID NO: 767) 37407 A_23_P135123 FRMD3 FERM domain contain- 0.509 CTGGTCTGAAGGGTCACGGGGCTGTCAACAGGTGTTC ing 3 CTTACTCATAATTGATTATTCAA (SEQ ID NO: 768) 32481 A_23_P59005 TAP1 transporter 1, ATP- 0.507 TCCAGGATGAGTTACTTGAAATTTGCCTTGAGTGTGTT binding cassette, sub- ACCTCCTTTCCAAGCTCCTCGT (SEQ ID NO: 769) family B 27197 A_24_P254933 ATXN2 ataxin 2 0.506 CCGACCATGTCCTGGTCCCTGTTCAACACCCACTTCAT GAATGCTGCCTGGGCTTCATAG (SEQ ID NO: 770) 29912 A_24_P326957 WDR23 WD repeat domain 23 0.506 TGGGTCTTTAGGGTAGGACAGGCTGTGGTATGAGAGG variant 1 CAGGAGTCTCCACAAGGCTTCAT (SEQ ID NO: 771) 26767 A_23_P356526 TRIM5 tripartite motif-con- 0.506 GAAGCCAGAAACTTTTCCAAAAAATCAAAGGAGAGTGT taining 5 variant TTCGAGCTCCTGATCTGAAAGG (SEQ ID NO: 772) delta 41790 A_23_P165636 CAPG capping protein (actin 0.506 CTGCTTGCTTGTCTGGCTGCCTGGTCAGTGCAGAGGT filament), gelsolin- GCCCGCTGCAGATGTTCAATAAA (SEQ ID NO: 773) like 38573 A_24_P127641 LOC441109 hypothetical gene sup- 0.503 TATATCGTAGGTGGCTTTAATACGTGTTATTTGCTCATC ported by AL713721 TGTATTTCTTACTCTTTGCAC (SEQ ID NO: 774) 40160 A_23_P88234 C14orf122 chromosome 14 ORF 122 0.503 GATAAGAACTTAGTGATGTGGAGGGACTGGGAAGAGT CACGGCAGATGGTGGGAGCTCTA (SEQ ID NO: 775) 9098 A_24_P383523 SAMD4 sterile alpha motif 0.501 CCATCTTCAGGGTTGCACAGAATCCTCCAAGATACTTT domain containing 4 GCAGCCTTTTTTCCCCCTGGTC (SEQ ID NO: 776) 16598 A_24_P242391 MPZL1 myelin protein zero- −0.501 GTGTATGCGGATATCCGAAAGAATTAAGAGAATACGTA like 1 variant 2 GAACATATCCTCAGCAAGAAAC (SEQ ID NO: 777) 39617 A_32_P109516 LOC389089 LOC389089 −0.507 TCCGTTTTTACAGCATTCTCGACCTGTGATTCTTGGTG GGGGAAACTAGTTATGTGGATA (SEQ ID NO: 778) 36575 A_23_P417282 MGC18216 hypothetical protein −0.507 AAATCAAACCAGAAGGCGGGATGGAATGGATGCACCG MGC 18216, clone CAAATAATGCATTTTCTGAGTTT (SEQ ID NO: 779) IMAGE: 4156235 34695 A_23_P403284 OTX1 orthodenticle homolog −0.517 TTAGTTGCTGTTGGTTGGTTGAACTGAACATATCTTGT 1 CTTAGCACCCAGGAAACAGAAC (SEQ ID NO: 780) 33205 A_24_P467358 EEF1G eukaryotic translation −0.526 CTGGATGCTTACTTGAAGACGAGGACTTTTCTGGTGG elongation factor 1 GCGAACGAGTGACATTGGCTGAC (SEQ ID NO: 781) gamma 25932 A_24_P87763 EEF2 eukaryotic translation −0.527 CATGTTTGTGGTCAAGGCCTATCTGCCCGTCAACGAG elongation factor 2 TCCTTTGGCTTCACCGCTGACCT (SEQ ID NO: 782) 14152 A_23_P124252 CAMK1D calcium/calmodulin- −0.528 TCCTGTTTGCCAGGCGCTTTCTATACTTAATCCCATGT dependent protein CATGCGACCCTAGGAC1TTTTT (SEQ ID NO: 783) kinase ID 35180 A_24_P177653 LOC340947 similar to bA508N22.1 −0.528 CATGAGTATTGATGAGAGCATTCACCTCCAGCGGTGG (HSPC025) GATAAATACAGCAACAAGATGCT (SEQ ID NO: 784) 38227 A_23_P104318 DDIT4 DNA-damage-inducible −0.529 TCGTGGAGGTGGTTTGTGTATCTTACTGGTCTGAAGG transcript 4 GACCAAGTGTGTTTGTTGTTTGT (SEQ ID NO: 785) 3684 A_23_P57521 EIF3S6IP eukaryotic TIF 3, −0.529 GAATTTCAGTCAGCCTCAGAGGTTGACTTCTACATTGA subunit 6 interacting TAAGGACATGATCCACATCGCG (SEQ ID NO: 786) protein 7635 A_32_P172917 LOC389832 similar to chromosome −0.530 AACTCAGCAGCAGCACTGCAGAATCTCCATGCCTGCA 2 ORF 27 CCTGCCCAAGGATTTATTCATAG (SEQ ID NO: 787) 39387 A_32_P76399 EIF3S6IP eukaryotic TIF 3, sub- −0.531 AGGTTGACTTCTACATTGATAAGGACATGATCCACATC unit 6 interacting GCGGACACCAAGGTCTCCAGGC (SEQ ID NO: 788) protein 24015 A_23_P105138 CAT catalase −0.532 CTCATCACTGGATGAAGATTCTCCTGTGCTAGATGTGC AAATGCAAGCTAGTGGCTTCAA (SEQ ID NO: 789) 15339 A_24_P8371 MYBBP1A MYB binding protein −0.536 GCTGCTGATTGTGAATCTCAGAGTCTTAAGAGAGAAG (P160)1a CCAAATATATTCCTCTTGTAAAT (SEQ ID NO: 790) 23589 A_24_P757154 ANP32A acidic (leucine-rich) −0.536 ACACTTTGCATGCTGGGTCAGGGAAGATTGTGGAGAG nuclear phosphoprotein AGGACAGTGCACCTGGTTTCCCC (SEQ ID NO: 791) 32 family, member A 19944 A_24_P32151 MGC45871 hypothetical protein −0.537 AAGGAAGTAAGGTACACCTCCTTGGTCAAGTACGACT MGC45871 CCGAGAGGCACTTCATCGACGAC (SEQ ID NO: 792) 11244 A_24_P154037 IRS2 insulin receptor sub- −0.540 GATGGTTCGTGTTCATACTGCAGCTTAAAACAAGCAAA strate 2 ATACACAGATGATAATATGCTA (SEQ 10 NO:793) 2728 A_32_P128258 SIGLECP3 sialic acid binding −0.543 ACTATGTGCCAGCATTTCCGTATGTGCAGAAGTTCATC Ig-like lectin, AATAGATATAGACTCAAAGAGC (SEQ ID NO: 794) pseudogene 3 43581 A_24_P717462 LOC651628 similar to Elongation −0.552 TGGATGAATGTGAGCAGAGTACCTTTGTGTTGGATAAA factor 1-gamma TTTCAGTGCAGGTACTCTAAGG (SEQ ID NO: 795) 24821 A_24_P136641 NDUFB6 NADH dehydrogenase −0.552 GCTAAGGAGGAAATACCCAGACAAAATCTTTGGGACG (ubiquinone) 1 beta AATGAAAATTTGTAACTCTTCTG (SEQ ID NO: 796) subcomplex, 6 26400 A_24_P588235 EIF3S6IP eukaryotic TIF 3, sub- −0.561 TGTGGATCATGTCCTTATCAATGTAGAAGTCAACCTCT unit 6 interacting GAGGCTGACTGAAATTCACCAT (SEQ ID NO: 797) protein 40567 A_23_P50081 IMPA2 inositol(myo)-1 (or −0.583 TAGCTGTTTCTCTCTTTAATCTCACGTAGCCTTTTTCAG 4)-monophosphatase 2 GTTAGTACGTGTTCTTCTGTC (SEQ ID NO: 798) 10228 A_24_P299318 FAM101B family with sequence −0.598 ACTTAATTTGAGCGAGTACCTTTTCATTTGACACTTTTC similarity 101, member CTGTTTCTAACCTTAGGAAAC (SEQ ID NO: 799) B 6063 A_24_P856176 EST highly conserved ge- −0.603 CCAGGCTGTGCAGTGGGTGAACTTTGCTGATGATAGC nomic region CAGTACCAGGGTGTTCCCACCTT (SEQ ID NO: 800) 14283 A_32_P159289 EST EST defined by −0.630 ACTGGCTTTTCTTTCATCTCTGGAGAGAGCTTGATTCG BE677474 TCATCTTATTGCTTTGTCTGAA (SEQ ID NO: 801) 19711 A_24_P554408 EFF1G eukaryotic translation −0.636 GGCAATGGCGTTGCTCTCAAACACACAGAATCCATCAT elongation factor 1 CACCCTCAAATGCTGGGACCTT (SEQ ID NO: 802) gamma

TABLE 3 Patient ABCoN ID Sample Date SLEDAI INFr Days from 1st Sample INFr Score 1 JHP004-01 QF1 Jul. 26, 2006 2 LOW 0 −2.813 JHP004-02 F Oct. 15, 2006 6 LOW 81 −1.864 2 JHP012-02 QF1 Sep. 10, 2006 0 LOW 0 −2.21 JHP012-04 F Nov. 5, 2006 8 LOW 56 −2.202 3 JHP017-02 QF1 Nov. 12, 2006 0 LOW 0 −2.44 JHP017-03 F Feb. 4, 2007 4 LOW 84 −2.07 4 JHP019-05 QF5 Mar. 8, 2007 0 LOW 0 0.255 JHP019-06 QF1 May 16, 2007 2 LOW 69 −0.219 JHP019-07 F Aug. 26, 2007 8 LOW 171 −0.124 5 JHP021-02 F Oct. 18, 2006 4 HIGH 0 2.882 JHP021-04 QF1 Dec. 19, 2006 0 HIGH 62 1.878 6 JHP023-01 QF4 Aug. 30, 2006 0 LOW 0 −1.684 JHP023-02 F Nov. 15, 2006 4 LOW 77 −1.404 JHP023-03 QF1 Feb. 14, 2007 0 LOW 168 −1.959 JHP023-04 F May. 9, 2007 8 LOW 252 −1.293 7 JHP028-01 QF5 Sep. 13, 2006 4 HIGH 0 2.883 JHP028-03 QF1 Mar. 18, 2007 4 HIGH 186 3.57 JHP028-04 F Jun. 17, 2007 16 HIGH 277 3.784 JHP028-05 QF4 Jul. 8, 2007 4 HIGH 298 4.696 JHP028-06 F Sep. 30, 2007 16 HIGH 382 4.325 8 JHP029-01 QF1 Sep. 13, 2006 4 HIGH 0 3.463 JHP029-03 F Mar. 7, 2007 9 HIGH 175 3.867 9 JHP030-03 F Feb. 4, 2007 12 LOW 0 1.392 JHP030-09 F Jun. 10, 2007 6 LOW 126 0.815 10 JHP033-02 QF1 Dec. 17, 2006 2 LOW 0 1.277 JHP033-03 F Mar. 4, 2007 12 HIGH 77 2.276 11 JHP039-02 QF1 Jan. 24, 2007 4 HIGH 0 4.707 JHP039-03 F Mar. 28, 2007 12 HIGH 63 4.281 12 JHP068-02 QF5 Apr. 8, 2007 0 HIGH 0 3.389 JHP068-03 QF1 Jul. 1, 2007 0 HIGH 84 3.773 JHP068-04 F Sep. 30, 2007 7 HIGH 175 3.992 13 JHP072-01 F Jan. 14, 2007 10 HIGH 0 3.178 JHP072-02 QF5 Apr. 15, 2007 0 LOW 91 0.155 JHP072-03 QF1 Jul. 15, 2007 0 HIGH 182 1.794 JHP072-04 F Oct. 7, 2007 8 HIGH 266 2.377 14 JHP074-01 QF1 Jan. 14, 2007 3 HIGH 0 3.087 JHP074-05 F Jan. 13, 2008 9 HIGH 364 4.226 15 JHP075-02 QF1 Oct. 7, 2007 1 LOW 0 −1.516 JHP075-03 F Jan. 13, 2008 11 LOW 98 −0.26 16 JHP078-01 QF5 Jan. 14, 2007 4 HIGH 0 3.381 JHP078-02 QF1 Jul. 22, 2007 4 HIGH 189 4.042 JHP078-03 F Dec. 12, 2007 10 HIGH 332 4.03 17 JHP079-02 F Feb. 28, 2007 4 LOW 0 −2.02 JHP079-03 QF4 Apr. 15, 2007 0 LOW 46 −2.095 JHP079-04 F Jul. 15, 2007 4 LOW 137 −1.931 18 JHP080-03 QF1 Jul. 18, 2007 4 HIGH 0 4.606 JHP080-04 F Sep. 12, 2007 8 HIGH 56 4.35 19 JHP081-01 QF5 Jan. 17, 2007 0 LOW 0 −2.31 JHP081-02 QF1 May 16, 2007 0 LOW 119 0.595 JHP081-03 F Jul. 18, 2007 4 LOW 182 −1.632 JHP081-04 QQ Oct. 17, 2007 0 LOW 273 −1.729 20 JHP100-01 QF1 May 16, 2007 4 HIGH 0 3.896 JHP100-03 F Mar. 26, 2008 12 HIGH 315 3.88 21 JHP102-01 QF5 May 20, 2007 4 HIGH 0 3.993 JHP102-02 QF1 Jun. 17, 2007 4 HIGH 28 4.048 JHP102-03 F Sep. 23, 2007 8 HIGH 126 3.19 JHP102-04 QF4 Dec. 23, 2007 0 HIGH 217 3.704 JHP102-05 F Feb. 20, 2008 4 HIGH 276 3.054 22 JHP104-01 QF5 Jun. 6, 2007 4 HIGH 0 4.508 JHP104-02 QF1 Sep. 5, 2007 4 HIGH 91 3.259 JHP104-04 F Feb. 27, 2008 12 HIGH 266 3.59 23 JHP111-02 QQ Sep. 12, 2007 0 HIGH 0 3.585 JHP111-04 QF1 Mar. 30, 2008 2 HIGH 200 3.503 JHP111-05 F Jun. 25, 2008 6 HIGH 287 2.196 24 JHP117-02 QF1 Sep. 30, 2007 0 LOW 0 −0.932 JHP117-03 F Dec. 19, 2007 4 LOW 80 0.251 25 JHP120-04 QQ Nov. 11, 2007 0 HIGH 0 3.736 JHP120-06 QF1 Apr. 27, 2008 0 HIGH 168 2.258 

We claim:
 1. A method of diagnosing a patient as having a longitudinally stable classification of SLE comprising: detecting the expression of two or more interferon response (INFr) genes in a sample from the patient; and diagnosing the patient as having type 1 or type 2 SLE based on analyzing the expression of the two or more genes using a statistical method, wherein expression of the two or more interferon response genes correlates with the expression of IFI27 from about 0.5 to about 1.0 and from about −0.5 to about −1.0 as calculated using a Pearson correlation.
 2. The method of claim 1 wherein at least one of the two or more genes is selected from the group consisting of the genes comprising SEQ ID NOs: 589-802.
 3. The method of claim 1 wherein the statistical method comprises a linear algorithm to produce an INFr score.
 4. The method of claim 3 wherein the INFr score is determined to be a high INFr score if the score is above an average of INFr scores taken from a plurality of patients, and the INFr score is determined to be a low INFr score if the score is below an average of INFr scores taken from a plurality of patients.
 5. The method of claim 4 wherein a high INFr score is correlated with type 1 SLE and a low INFr score is correlated with type 2 SLE.
 6. The method of claim 3 wherein the linear algorithm comprises IFI27 +IFI144*(1.1296) +OAS3*(1.8136).
 7. The method of claim 1 further comprising assigning the patient to a clinical trial based on the diagnosis of type 1 or type 2 SLE.
 8. The method of claim 1 further comprising monitoring the status of the patient based on the diagnosis of type 1 or type 2 SLE.
 9. The method of claim 8 wherein the status of the patient is incipient flare or disease activity.
 10. The method of claim 8 wherein the status of the patient comprises a response to a therapeutic agent administered to the patient.
 11. The method of claim 10 wherein the therapeutic agent is selected from the group consisting of ACE inhibitors, aspirin, azathioprine, B7RP-1-fc,β-blockers, brequinar sodium, campath-1H, celecoxib, chloroquine, corticosteroids, warfarin, cyclophosphamide, cyclosporin A, dehydroepiandrosterone, deoxyspergualin, dexamethasone, diclofenac, diflunisal, etodolac, everolimus, FK778, piroxicam, fenoprofen, flurbiprofen, heparin, hydralazine, hydroxychloroquine, CTLA-4 or LFA3 immunoglobulin, ibuprofen, indomethacin, ISAtx-247, ketoprofen, ketorolac, leflunomide, meclophenamate, mefenamic acid, mepacrine, 6-mercaptopurine, meloxicam, methotrexate, mizoribine, mycophenolate mofetil, naproxen, oxaprozin, hydroxychloroquine, NOX-100, prednisone, methylprednisolone, rapamycin (sirolimus), sulindac, tacrolimus anti-thymocyte globulin, tolmetin, tresperimus, U0126, and antibodies including but not limited to alpha lymphocyte antibodies, adalimumab, anti-CD3, anti-CD25, anti-CD52, anti-IL2R, and anti-TAC antibodies, basiliximab, daclizumab, etanercept, hu5C8, infliximab, OKT4, and natalizumab.
 12. The method of claim 8 wherein the status of the patient comprises a response to an immunosuppressant administered to the patient.
 13. The method of claim 12 wherein the immunosuppressant is selected from the group consisting of aspirin, azathioprine, chloroquine, corticosteroids, cyclophosphamide, cyclosporin A, dehydroepiandrosterone, deoxyspergualin, dexamethasone, everolimus, fenoprofen, hydralazine, hydroxychloroquine, immunoglobulin, ibuprofen, indomethacin, leflunomide, ketoprofen, meclophenamate, mepacrine, 6-mercaptopurine, methotrexate, mizoribine, mycophenolate mofetil, naproxen, prednisone, methylprednisolone, rapamycin (sirolimus), methylprednisolone sodium succinate, tacrolimus, anti-thymocyte globulin, tolmetin, tresperimus, and triamcinolone.
 14. A method for predicting flare in a patient diagnosed with SLE comprising: analyzing expression in a sample from the patient to produce a gene expression profile wherein a first portion of the analysis comprises using the expression of at least one gene selected from each of at least two of the clusters 1 through 15 of Table 1 and at least one statistical method to produce a patient gene expression profile, and a second portion of the analysis comprises using expression of at least two interferon response genes and a linear algorithm to classify the patient as having type 1 SLE or type 2 SLE, wherein expression of the two or more interferon response genes correlates with the expression of IFI27 from about 0.5 to about 1.0 and from about −0.5 to about −1.0 as calculated using a Pearson correlation; and predicting flare by comparing the patient gene expression profile to at least one reference profile.
 15. The method of claim 14 wherein the at least two INFr genes are selected from the group consisting of the genes comprising SEQ ID NOs: 589-802.
 16. The method of claim 14 wherein the at least one reference profile is selected from the group consisting of at least one normal subject, at least one patient classified as having type 1 SLE with quiescent status, at least one patient classified as having type 1 SLE in flare, at least one patient classified as having type 2 SLE with quiescent status, and at least one patient classified as having type 2 SLE in flare. 